Anti-Human CD52 Immunoglobulins

ABSTRACT

The present invention relates to humanized immunoglobulins, mouse monoclonal antibodies and chimeric antibodies that have binding specificity for human CD52. The present invention further relates to a humanized immunoglobulin light chain and a humanized immunoglobulin heavy chain. The invention also relates to isolated nucleic acids, recombinant vectors and host cells that comprise a sequence which encodes a humanized immunoglobulin or immunoglobulin light chain or heavy chain, and to a method of preparing a humanized immunoglobulin. The humanized immunoglobulins can be used in therapeutic applications to treat, for example, autoimmune disease, cancer, non-Hodgkin&#39;s lymphoma, multiple sclerosis and chronic lymphocytic leukemia.

This application is a continuation application of U.S. patent application Ser. No. 14/864,736, filed Sep. 24, 2015, which is a continuation application of U.S. patent application Ser. No. 14/091,083, filed Nov. 26, 2013 (now abandoned), which is a continuation of U.S. patent application Ser. No. 13/320,019, filed Nov. 10, 2011 (now issued as U.S. Pat. No. 8,617,554), which is a national stage application under 35 U.S.C. § 371 of International Application PCT/US2010/034704 (now expired), filed May 13, 2010, which claims priority from U.S. Provisional Application 61/177,837 (now expired), filed May 13, 2009. The contents of the foregoing priority applications are incorporated by reference herein in their entirety.

A sequence listing associated with this application is being submitted electronically via EFS-Web in text format, and is hereby incorporated by reference in its entirety into the specification. The name of the text file containing the Sequence Listing is 022548_C3029_SL.txt. The text file, created on Apr. 9, 2019, is 182,335 bytes in size.

BACKGROUND OF THE INVENTION

CD52 is a glycosylated, glycosylphosphatidylinositol (GPI)-anchored cell surface protein found in abundance (500,000 molecules/cell) on a variety of normal and malignant lymphoid cells (e.g., T and B cells). See, e.g., Hale et al., J Biol regul Homeost Agents 15:386-391 (2001); Huh et al., Blood 92: Abstract 4199 (1998); Elsner et al., Blood 88:4684-4693 (1996); Gilleece et al., Blood 82:807-812 (1993); Rodig et al., Clin Cancer Res 12:7174-7179 (2006); Ginaldi et al., Leuk Res 22:185-191 (1998). CD52 is expressed at lower levels on myeloid cells such as monocytes, macrophages, and dendritic cells, with little expression found on mature natural killer (NK) cells, neutrophils, and hematological stem cells. Id. CD52 is also produced by epithelial cells in the epididymis and duct deferens, and is acquired by sperm during passage through the genital tract (Hale et al., 2001, supra; Domagala et al., Med Sci Monit 7:325-331 (2001)). The exact biological function of CD52 remains unclear but some evidence suggests that it may be involved in T cell migration and co-stimulation (Rowan et al., Int Immunol 7:69-77 (1995); Masuyama et al., J Exp Med 189:979-989 (1999); Watanabe et al., Clin Immunol 120:247-259 (2006)).

Campath-1H® (alemtuzumab, Campath®, MabCampath®) is a humanized anti-human CD52 monoclonal antibody that exhibits potent in vitro cytotoxic effects (antibody-dependent cell mediated cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC)). Campath® recognizes an epitope which consists of the carboxy terminal four amino acids of the mature CD52 protein and a portion of the negatively charged GPI anchor. Due to its significant cytotoxic effects, Campath® is capable of depleting CD52 positive cells in vivo and it is approved for front line and third line treatment of chronic lymphocytic leukemia (CLL). Campath® has been evaluated for its utility in the treatment of several autoimmune diseases, including rheumatoid arthritis, vasculitis, myositis and Wegener's disease. However, the most advanced studies of Campath® are in treating relapsing remitting multiple sclerosis (MS). These studies showed a significant improvement in time to relapse relative to an active comparator (Rebif® (i.e., interferon beta-1a)).

A need exists for additional therapeutic agents and approaches to target CD52.

SUMMARY OF THE INVENTION Humanized Immunoglobulins

The invention relates to humanized immunoglobulins that have binding specificity for human CD52 (huCD52). They may comprise the complementarity determining regions (CDRs) of mouse anti-human CD52 antibodies. The humanized immunoglobulins of the invention have amino acid sequences that are different from other humanized immunoglobulins, and in particular from other humanized immunoglobulins that comprise CDRs of murine anti-human CD52 antibodies. The humanized immunoglobulins of the invention are different from the humanized immunoglobulin Campath®. In some embodiments, they provide advantages over humanized antibodies that comprise the CDRs of Campath®.

The humanized immunoglobulins described herein can comprise a humanized heavy chain and a humanized light chain. In one embodiment, the humanized immunoglobulin comprises a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 3 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 16; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 4 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 17; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 5 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 18; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 6 and a heavy chain comprising one or more CDRs of SEQ ID NO: 19; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 7 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 20; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 8 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 21; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 9 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 22; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 10 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 23; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 11 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 24; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 12 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 25; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 12 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 137; or a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 13 and a heavy chain sequence comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 26. The CDRs in the above-mentioned SEQ ID NOs are indicated by FIGS. 2 and 3 and are referred to in Tables 1-6 as provided herein.

In another embodiment, the humanized immunoglobulin that has binding specificity for human CD52 comprises a light chain comprising one or more CDRs (e.g., all three) selected from the group consisting of SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 29, SEQ ID NO: 30, SEQ ID NO: 31, SEQ ID NO: 32, SEQ ID NO: 33, SEQ ID NO: 34, SEQ ID NO: 35, SEQ ID NO: 36, SEQ ID NO: 37, SEQ ID NO: 38, SEQ ID NO: 39, SEQ ID NO: 40, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43, SEQ ID NO: 44, SEQ ID NO: 45, SEQ ID NO: 46, SEQ ID NO: 47, and SEQ ID NO: 48; a heavy chain comprising one or more CDRs (e.g., all three) selected from the group consisting of SEQ ID NO: 49, SEQ ID NO: 50, SEQ ID NO: 51, SEQ ID NO: 52, SEQ ID NO: 53, SEQ ID NO: 54, SEQ ID NO: 55, SEQ ID NO: 56, SEQ ID NO: 57, SEQ ID NO: 58, SEQ ID NO: 59, SEQ ID NO: 60, SEQ ID NO: 61, SEQ ID NO: 62, SEQ ID NO: 63, SEQ ID NO: 64, SEQ ID NO: 65, SEQ ID NO: 66, SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO: 69, SEQ ID NO: 70, SEQ ID NO: 71, SEQ ID NO: 72, SEQ ID NO: 73, SEQ ID NO: 74, and SEQ ID NO: 294; or such a light chain and such a heavy chain; wherein the humanized immunoglobulin is not Campath®.

In another embodiment, the humanized immunoglobulin that has a binding specificity for human CD52 comprises a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, or SEQ ID NO: 13; a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25, SEQ ID NO: 26, or SEQ ID NO: 137; or such a light chain and such a heavy chain; wherein the humanized immunoglobulin is not Campath®.

In some embodiments, the framework region of the humanized immunoglobulin has at least 50% homology to the framework region of the immunoglobulin from which the light chain CDRs and the heavy chain CDRs are obtained. For example, the framework region of the humanized immunoglobulin can be at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, at least 98%, at least 99%, or even 100% identical, to a germline human immunoglobulin sequence. In one embodiment, the framework region of the humanized immunoglobulin can be obtained or derived from an IgG human antibody variable region. In another embodiment the CD52 is wildtype human CD52. In yet another embodiment, the humanized immunoglobulin can compete with alemtuzumab for binding to human CD52, e.g., it can bind to an epitope that is identical to, or which overlaps with, the epitope to which alemtuzumab binds.

The invention also relates to a humanized light chain of a humanized immunoglobulin of the invention. In one embodiment, the humanized light chain comprises one or more CDRs selected from the group consisting of SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 29, SEQ ID NO: 30, SEQ ID NO: 31, SEQ ID NO: 32, SEQ ID NO: 33, SEQ ID NO: 34, SEQ ID NO: 35, SEQ ID NO: 36, SEQ ID NO: 37, SEQ ID NO: 38, SEQ ID NO: 39, SEQ ID NO: 40, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43, SEQ ID NO: 44, SEQ ID NO: 45, SEQ ID NO: 46, SEQ ID NO: 47, and SEQ ID NO: 48 or a combination thereof, wherein the humanized light chain is not the humanized light chain of Campath®.

In other embodiment, the humanized light chain comprises one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12 or SEQ ID NO: 13, wherein the humanized light chain is not the humanized light chain of Campath®.

The invention also relates to a humanized heavy chain of a humanized immunoglobulin of the invention. In one embodiment, the humanized heavy chain comprises one or more CDRs of an Ig variable domain selected from the group consisting of SEQ ID NO: 49, SEQ ID NO: 50, SEQ ID NO: 51, SEQ ID NO: 52, SEQ ID NO: 53, SEQ ID NO: 54, SEQ ID NO: 55, SEQ ID NO: 56, SEQ ID NO: 57, SEQ ID NO: 58, SEQ ID NO: 59, SEQ ID NO: 60, SEQ ID NO: 61, SEQ ID NO: 62, SEQ ID NO: 63, SEQ ID NO: 64, SEQ ID NO: 65, SEQ ID NO: 66, SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO: 69, SEQ ID NO: 70, SEQ ID NO: 71, SEQ ID NO: 72, SEQ ID NO: 73, SEQ ID NO: 74, and SEQ ID NO: 294, or a combination thereof, wherein the humanized heavy chain is not the humanized heavy chain of Campath®.

In other embodiments, the humanized heavy chain comprises one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25, SEQ ID NO: 26, or SEQ ID NO: 137, wherein the humanized heavy chain is not the humanized heavy chain of Campath®.

Preferably, the humanized immunoglobulins of the present invention comprise both a humanized light chain of the invention and a humanized heavy chain of the invention.

In other embodiments, the invention provides a humanized immunoglobulin which binds to the same epitope on human CD52 as, or competes or cross-competes with, a mouse monoclonal antibody comprising a light chain variable region of SEQ ID NO: 3 and a heavy chain variable region of SEQ ID NO: 16; a light chain variable region of SEQ ID NO: 4 and a heavy chain variable region of SEQ ID NO: 17; a light chain variable region of SEQ ID NO: 5 and a heavy chain variable region of SEQ ID NO: 18; a light chain variable region of SEQ ID NO: 6 and a heavy chain variable region of SEQ ID NO: 19; a light chain variable region of SEQ ID NO: 7 and a heavy chain variable region of SEQ ID NO: 20; a light chain variable region of SEQ ID NO: 8 and a heavy chain variable region of SEQ ID NO: 21; a light chain variable region of SEQ ID NO: 9 and a heavy chain variable region of SEQ ID NO: 22; a light chain variable region of SEQ ID NO: 10 and a heavy chain variable region of SEQ ID NO: 23; a light chain variable region of SEQ ID NO: 11 and a heavy chain variable region of SEQ ID NO: 24; a light chain variable region of SEQ ID NO: 12 and a heavy chain variable region of SEQ ID NO: 25; or a light chain variable region of SEQ ID NO: 13 and a heavy chain variable region of SEQ ID NO: 26. In other embodiments, the humanized immunoglobulin binds to an epitope on human CD52 which overlaps with the epitope to which such a mouse monoclonal antibody binds.

In other embodiments, the invention provides a humanized immunoglobulin which binds to an epitope on human CD52 (e.g., SEQ ID NO: 104) comprising at least residue 1 of the mature human CD52 sequence (where residue 1 is the N-terminus of the mature human CD52 sequence, i.e., the N-terminal glycine [G] residue; see FIG. 4). The humanized immunoglobulin may bind to an epitope comprising at least residues 1, 3, 4 and 5 of the mature human CD52 sequence (these residues being a glycine [G], an asparagine [N], an aspartate [D], and a threonine [T], respectively). The humanized immunoglobulin may bind to an epitope comprising at least residues 1, 2, 3, 4 and 5 of the mature human CD52 sequence (these residues being a glycine [G], a glutamine [Q], an asparagine [N], an aspartate [D], and a threonine [T], respectively). In other embodiments, the invention provides a humanized immunoglobulin which binds to an epitope on human CD52 comprising at least residues 7, 8 and 9 of the mature human CD52 sequence (these residues being a glutamine [Q], a threonine [T], and a serine [S], respectively). In some embodiments, the epitope comprises at least residues 7 (Q), 8 (T) and 11 (P) of the mature human CD52 sequence. In some embodiments, the epitope comprises at least residues 4 (D) and 11 (P) of the mature human CD52 sequence.

In some embodiments, the invention provides a humanized immunoglobulin, which binds to human CD52, and which comprises a light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 115, SEQ ID NO: 118, and SEQ ID NO: 121 (e.g., all three of said CDRs), or a heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 124, SEQ ID NO: 127, and SEQ ID NO: 130 (e.g., all three of said CDRs), or both such light chain and such heavy chain. In other embodiments, the invention provides a humanized immunoglobulin, which binds to human CD52, and which comprises a light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 116, SEQ ID NO: 119, and SEQ ID NO: 122 (e.g., all three of said CDRs), or a heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 125, SEQ ID NO: 128, and SEQ ID NO: 131 (e.g., all three of said CDRs), or both such light chain and heavy chain. In still further embodiments, the invention provides a humanized immunoglobulin, which binds to human CD52, and which comprises a light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 117, SEQ ID NO: 120, and SEQ ID NO: 123 (e.g., all three of said CDRs), or a heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 126, SEQ ID NO: 129, and SEQ ID NO: 132 (e.g., all three of said CDRs), or both such light chain and such heavy chains.

In certain embodiments, the humanized immunoglobulin comprises a light chain comprising the CDRs of SEQ ID NO: 115, SEQ ID NO: 118 and SEQ ID NO: 121 and a heavy chain comprising the CDRs of SEQ ID NO: 124, SEQ ID NO: 127 and SEQ ID NO: 130. In other embodiments, the humanized immunoglobulin comprises a light chain comprising the CDRs of SEQ ID NO: 116, SEQ ID NO: 119 and SEQ ID NO: 122 and a heavy chain comprising the CDRs of SEQ ID NO: 125, SEQ ID NO: 128 and SEQ ID NO: 131. In other embodiments, the humanized immunoglobulin comprises a light chain comprising the CDRs of SEQ ID NO: 117, SEQ ID NO: 120 and SEQ ID NO: 123 and a heavy chain comprising the CDRs of SEQ ID NO: 126, SEQ ID NO: 129 and SEQ ID NO: 132.

The humanized immunoglobulins of the present invention are different from the humanized immunoglobulin Campath®.

The amino acid sequences of the above-mentioned SEQ ID NOs: 115-132 are provided below, and are based on the amino acid sequences that are reported in Tables 1-6 as provided elsewhere herein. In these amino acid sequences, “X” stands for any amino acid, and the symbol “/” indicates that either (or any) of the amino acids depicted adjacent that symbol may be present at the indicated position (e.g., K/R indicates that a lysine or arginine residue is present at the indicated position and F/L/V indicates that a phenylalanine, leucine or valine residue is present at the indicated position).

Light Chain CDR-1 Sequences (SEQ ID NO: 115) K/RSSQSLLN/IXS/TN/DGXS/TYLX (SEQ ID NO: 116) K/RSSQSLL/V/IHS/TNGXS/TYLH (SEQ ID NO: 117) RSSQSLVHTNGNS/TYLH Light Chain CDR-2 Sequences (SEQ ID NO: 118) XVSXXXS (SEQ ID NO: 119) XVSXRXS (SEQ ID NO: 120) MVSXRFS Light Chain CDR-3 Sequences (SEQ ID NO: 121) XQXXH/R/KF/LN/IXX (SEQ ID NO: 122) SQSXH/R/KF/LN/IPX (SEQ ID NO: 123) SQSXHVPF/P Heavy Chain CDR-1 Sequences (SEQ ID NO: 124) GFXFXXYW/YMX (SEQ ID NO: 125) GFTFXXYW/YMX (SEQ ID NO: 126) GFTFTDYW/YMS Heavy Chain CDR-2 Sequences (SEQ ID NO: 127) XIRXKXBXYXTXYXXSVKG (SEQ ID NO: 128) XIRXKXNXYTTEYXXSVKG (SEQ ID NO: 129) FIRNKANGYTTEYXXSVKG Heavy Chain CDR-3 Sequences (SEQ ID NO: 130) TXXXY/F/W (SEQ ID NO: 131) TRYXY/F/WFDY (SEQ ID NO: 132) TRYIF/WFDY

The invention also relates to a humanized light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 115, SEQ ID NO: 118, and SEQ ID NO: 121 (e.g., all three of said CDRs); a humanized light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 116, SEQ ID NO: 119, and SEQ ID NO: 122 (e.g., all three of said CDRs); or a humanized light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 117, SEQ ID NO: 120, and SEQ ID NO: 123 (e.g., all three of said CDRs).

The invention also relates to a humanized heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 124, SEQ ID NO: 127, and SEQ ID NO: 130 (e.g., all three of said CDRs); a humanized heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 125, SEQ ID NO: 128, and SEQ ID NO: 131 (e.g., all three of said CDRs); or a humanized heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 126, SEQ ID NO: 129, and SEQ ID NO: 132 (e.g., all three of said CDRs).

The humanized light chains and humanized heavy chains of the present invention are different from the humanized light chain and the humanized heavy chains of the humanized immunoglobulin Campath®.

In some embodiments of the present invention, the humanized immunoglobulins of the invention (irrespective of the manner in which they might otherwise be defined, e.g., regardless of whether they might also be defined in terms of the sequence of one or more of their CDRs and/or by their cross-reactivity with a mouse monoclonal antibody or another humanized immunoglobulin): (1) exhibit binding to glycosylated and de-glycosylated CD52 with no apparent preference; (2) exhibit binding specific for glycosylated CD52; (3) exhibit binding specific for de-glycosylated CD52; or (4) exhibit binding preferential for de-glycosylated over glycosylated CD52. In certain embodiments, the humanized immunoglobulins of the invention have a greater binding affinity for glycosylated human CD52 than for non-glycosylated or de-glycosylated human CD52. Indeed, in certain embodiments of the present invention, the humanized immunoglobulins of the present invention exhibit binding that is specific for glycosylated human CD52. Binding affinity for non-glycosylated or de-glycosylated human CD52 may be determined with the use of mature human CD52 that has been de-glycosylated using a glycosidase, e.g., using the endoglycosidase PNGase-F. In certain embodiments of the present invention, the humanized immunoglobulins of the invention bind to an epitope on mature human CD52 which comprises its N-linked carbohydrate moiety. This carbohydrate moiety is a sialylted, polylactosamine-containing core-fucosylated tetraantennary N-linked oligosaccharide (Treumann, A. et al., (1995) J Biol. Chem. 270:6088-6099). This epitope may also comprise at least residue 1 of the mature human CD52 sequence, at least residue 3 of the mature human CD52 sequence, at least residues 1, 3, 4 and 5 of the mature human CD52 sequence, or at least residues 1, 2, 3, 4 and 5 of the mature human CD52 sequence. In some embodiments, the mouse or chimeric antibodies of the present invention may have any of these binding features.

Isolated nucleic acid molecules that encode a humanized immunoglobulin, humanized light chain or humanized heavy chain of the invention, as defined elsewhere herein, are also provided. In some embodiments, the invention is an (one or more) isolated nucleic acid molecule encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized light chain comprises one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 3 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 16; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 4 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 17; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 5 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 18; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 6 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 19; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 7 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 20; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 8 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 21; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 9 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 22; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 10 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 23; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 11 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 24; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 12 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 25; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 12 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 137; or a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 13 and a heavy chain sequence comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 26.

In some embodiments, the invention is one or more isolated nucleic acid molecules encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin binds to the same epitope on human CD52 as a mouse monoclonal antibody comprising a light chain variable region of SEQ ID NO: 3 and a heavy chain variable region of SEQ ID NO: 16; a light chain variable region of SEQ ID NO: 4 and a heavy chain variable region of SEQ ID NO: 17; a light chain variable region of SEQ ID NO: 5 and a heavy chain variable region of SEQ ID NO: 18; a light chain variable region of SEQ ID NO: 6 and a heavy chain variable region of SEQ ID NO: 19; a light chain variable region of SEQ ID NO: 7 and a heavy chain variable region of SEQ ID NO: 20; a light chain variable region of SEQ ID NO: 8 and a heavy chain variable region of SEQ ID NO: 21; a light chain variable region of SEQ ID NO: 9 and a heavy chain variable region of SEQ ID NO: 22; a light chain variable region of SEQ ID NO: 10 and a heavy chain variable region of SEQ ID NO: 23; a light chain variable region of SEQ ID NO: 11 and a heavy chain variable region of SEQ ID NO: 24; a light chain variable region of SEQ ID NO: 12 and a heavy chain variable region of SEQ ID NO: 25; or a light chain variable region of SEQ ID NO: 13 and a heavy chain variable region of SEQ ID NO: 26. In other embodiments, the invention is one or more isolated nucleic acid molecules encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin binds to an epitope on human CD52 which overlaps with the epitope to which such a mouse monoclonal antibody binds.

In other embodiments, the invention is one or more isolated nucleic acid molecules encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin binds to an epitope comprising at least residue 1 of mature human CD52; the humanized immunoglobulin binds to an epitope comprising at least residues 1, 3, 4 and 5 of mature human CD52; the humanized immunoglobulin binds to an epitope comprising at least residues 1, 2, 3, 4 and 5 of mature human CD52; or the humanized immunoglobulin binds to an epitope comprising at least residues 7, 8 and 9 of mature human CD52. In some embodiments, the epitope comprises at least residues 7, 8 and 11 of the mature human CD52 sequence. In some embodiments, the epitope comprises at least residues 4 and 11 of the mature human CD52 sequence.

In other embodiments, the invention is one or more isolated nucleic acid molecules encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin comprises a light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 115, SEQ ID NO: 118, and SEQ ID NO: 121 (e.g., all three of said CDRs), and/or a heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 124, SEQ ID NO: 127, and SEQ ID NO: 130 (e.g., all three of said CDRs); a light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 116, SEQ ID NO: 119, and SEQ ID NO: 122 (e.g., all three of said CDRs), and/or a heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 125, SEQ ID NO: 128, and SEQ ID NO: 131 (e.g., all three of said CDRs); or a light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 117, SEQ ID NO: 120, and SEQ ID NO: 123 (e.g., all three of said CDRs), and/or a heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 126, SEQ ID NO: 129, and SEQ ID NO: 132 (e.g., all three of said CDRs).

In certain embodiments, the invention is one or more isolated nucleic acid molecules encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin comprises a light chain comprising the CDRs of SEQ ID NO: 115, SEQ ID NO: 118 and SEQ ID NO: 121 and a heavy chain comprising the CDRs of SEQ ID NO: 124, SEQ ID NO: 127 and SEQ ID NO: 130; a light chain comprising the CDRs of SEQ ID NO: 116, SEQ ID NO: 119 and SEQ ID NO: 122 and a heavy chain comprising the CDRs of SEQ ID NO: 125, SEQ ID NO: 128 and SEQ ID NO: 131; or a light chain comprising the CDRs of SEQ ID NO: 117, SEQ ID NO: 120 and SEQ ID NO: 123 and a heavy chain comprising the CDRs of SEQ ID NO: 126, SEQ ID NO: 129 and SEQ ID NO: 132.

The one or more nucleic acids of the invention do not encode the humanized immunoglobulin Campath®.

In other embodiments, the invention is one or more isolated nucleic acid molecules encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin has a greater binding affinity for glycosylated human CD52 than for non-glycosylated or de-glycosylated human CD52, e.g., exhibits binding that is specific for glycosylated human CD52. The humanized immunoglobulin may bind to an epitope on mature human CD52 which comprises its N-linked carbohydrate moiety. This epitope may also comprise at least residue 1 of the mature human CD52 sequence, at least residue 3 of the mature human CD52 sequence, at least residues 1, 3, 4 and 5 of the mature human CD52 sequence, or at least residues 1, 2, 3, 4 and 5 of the mature human CD52 sequence.

In other embodiments, the invention is an isolated nucleic acid molecule encoding a humanized light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12 or SEQ ID NO: 13, wherein the humanized light chain is not the humanized light chain of Campath®.

In other embodiments, the invention is an isolated nucleic acid molecule encoding a humanized heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25, SEQ ID NO: 26, or SEQ ID NO: 137, wherein the humanized heavy chain is not the humanized heavy chain of Campath®.

In other embodiments, the invention is an isolated nucleic acid molecule encoding a humanized light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 29, SEQ ID NO: 30, SEQ ID NO: 31, SEQ ID NO: 32, SEQ ID NO: 33, SEQ ID NO: 34, SEQ ID NO: 35, SEQ ID NO: 36, SEQ ID NO: 37, SEQ ID NO: 38, SEQ ID NO: 39, SEQ ID NO: 40, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43, SEQ ID NO: 44, SEQ ID NO: 45, SEQ ID NO: 46, SEQ ID NO: 47, and SEQ ID NO: 48, or a combination thereof, wherein the humanized light chain is not the humanized light chain of Campath®.

In other embodiments, the invention is an isolated nucleic acid molecule encoding a humanized heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 49, SEQ ID NO: 50, SEQ ID NO: 51, SEQ ID NO: 52, SEQ ID NO: 53, SEQ ID NO: 54, SEQ ID NO: 55, SEQ ID NO: 56, SEQ ID NO: 57, SEQ ID NO: 58, SEQ ID NO: 59, SEQ ID NO: 60, SEQ ID NO: 61, SEQ ID NO: 62, SEQ ID NO: 63, SEQ ID NO: 64, SEQ ID NO: 65, SEQ ID NO: 66, SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO: 69, SEQ ID NO: 70, SEQ ID NO: 71, SEQ ID NO: 72, SEQ ID NO: 73, SEQ ID NO: 74, and SEQ ID NO: 294, or a combination thereof, wherein the humanized heavy chain is not the humanized heavy chain of Campath®.

In other embodiments, the invention is an isolated nucleic acid molecule encoding a humanized light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 115, SEQ ID NO: 118, and SEQ ID NO: 121 (e.g., all three of said CDRs); a humanized light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 116, SEQ ID NO: 119, and SEQ ID NO: 122 (e.g., all three of said CDRs); or a humanized light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 117, SEQ ID NO: 120, and SEQ ID NO: 123 (e.g., all three of said CDRs).

In other embodiments, the invention is an isolated nucleic acid molecule encoding a humanized heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 124, SEQ ID NO: 127, and SEQ ID NO: 130 (e.g., all three of said CDRs); a humanized heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 125, SEQ ID NO: 128, and SEQ ID NO: 131 (e.g., all three of said CDRs); or a humanized heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 126, SEQ ID NO: 129, and SEQ ID NO: 132 (e.g., all three of said CDRs).

The invention also relates to recombinant vectors (e.g., expression vectors, including mammalian cell expression vectors) that comprise a nucleic acid encoding a humanized immunoglobulin (e.g., a humanized light chain and a humanized heavy chain), a humanized light chain, or a humanized heavy chain of the invention. In some embodiments, the invention is a recombinant vector comprising a nucleic acid encoding a humanized immunoglobulin that comprises a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 3 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 16; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 4 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 17; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 5 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 18; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 6 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 19; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 7 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 20; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 8 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 21; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 9 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 22; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 10 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 23; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 11 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 24; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 12 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 25; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 12 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 137; or a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 13 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 26.

In other embodiments, the recombinant vector comprises a nucleic acid encoding a humanized light chain, wherein the humanized light chain comprises one or more CDRs selected from the group consisting of SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 29, SEQ ID NO: 30, SEQ ID NO: 31, SEQ ID NO: 32, SEQ ID NO: 33, SEQ ID NO: 34, SEQ ID NO: 35, SEQ ID NO: 36, SEQ ID NO: 37, SEQ ID NO: 38, SEQ ID NO: 39, SEQ ID NO: 40, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43, SEQ ID NO: 44, SEQ ID NO: 45, SEQ ID NO: 46, SEQ ID NO: 47, and SEQ ID NO: 48, or a combination thereof, wherein the humanized light chain is not the humanized light chain of Campath®.

In other embodiments, the recombinant vector comprises a nucleic acid encoding a humanized heavy chain, wherein the humanized heavy chain comprises one or more CDRs selected from the group consisting of SEQ ID NO: 49, SEQ ID NO: 50, SEQ ID NO: 51, SEQ ID NO: 52, SEQ ID NO: 53, SEQ ID NO: 54, SEQ ID NO: 55, SEQ ID NO: 56, SEQ ID NO: 57, SEQ ID NO: 58, SEQ ID NO: 59, SEQ ID NO: 60, SEQ ID NO: 61, SEQ ID NO: 62, SEQ ID NO: 63, SEQ ID NO: 64, SEQ ID NO: 65, SEQ ID NO: 66, SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO: 69, SEQ ID NO: 70, SEQ ID NO: 71, SEQ ID NO: 72, SEQ ID NO: 73, SEQ ID NO: 74, and SEQ ID NO: 294, or a combination thereof, wherein the humanized light chain is not the humanized light chain of Campath®.

In some embodiments, the invention provides a recombinant vector comprising a nucleic acid molecule, or a pair of recombinant vectors comprising nucleic acid molecules, encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin binds to the same epitope on human CD52 as a mouse monoclonal antibody comprising a light chain variable region of SEQ ID NO: 3 and a heavy chain variable region of SEQ ID NO: 16; a light chain variable region of SEQ ID NO: 4 and a heavy chain variable region of SEQ ID NO: 17; a light chain variable region of SEQ ID NO: 5 and a heavy chain variable region of SEQ ID NO: 18; a light chain variable region of SEQ ID NO: 6 and a heavy chain variable region of SEQ ID NO: 19; a light chain variable region of SEQ ID NO: 7 and a heavy chain variable region of SEQ ID NO: 20; a light chain variable region of SEQ ID NO: 8 and a heavy chain variable region of SEQ ID NO: 21; a light chain variable region of SEQ ID NO: 9 and a heavy chain variable region of SEQ ID NO: 22; a light chain variable region of SEQ ID NO: 10 and a heavy chain variable region of SEQ ID NO: 23; a light chain variable region of SEQ ID NO: 11 and a heavy chain variable region of SEQ ID NO: 24; a light chain variable region of SEQ ID NO: 12 and a heavy chain variable region of SEQ ID NO: 25; or a light chain variable region of SEQ ID NO: 13 and a heavy chain variable region of SEQ ID NO: 26. In other embodiments, the invention provides a recombinant vector comprising a nucleic acid molecule, or a pair of recombinant vectors comprising nucleic acid molecules, encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin binds to an epitope on human CD52 which overlaps with the epitope to which such a mouse monoclonal antibody binds.

In other embodiments, the recombinant vector comprises a nucleic acid molecule, or a pair of recombinant vectors comprise nucleic acid molecules, encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin binds to an epitope comprising at least residue 1 of mature human CD52; binds to an epitope comprising at least residues 1, 3, 4 and 5 of mature human CD52; binds to an epitope comprising at least residues 1, 2, 3, 4 and 5 of mature human CD52; or binds to an epitope comprising at least residues 7, 8 and 9 of mature human CD52. In some embodiments, the epitope comprises at least residues 7, 8 and 11 of the mature human CD52 sequence. In some embodiments, the epitope comprises at least residues 4 and 11 of the mature human CD52 sequence.

In some embodiments, the recombinant vector comprises a nucleic acid molecule, or a pair of recombinant vectors comprise nucleic acid molecules, encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin comprises a light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 115, SEQ ID NO: 118, and SEQ ID NO: 121 (e.g., all three of said CDRs), and/or a heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 124, SEQ ID NO: 127, and SEQ ID NO: 130 (e.g., all three of said CDRs); a light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 116, SEQ ID NO: 119, and SEQ ID NO: 122 (e.g., all three of said CDRs), and/or a heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 125, SEQ ID NO: 128, and SEQ ID NO: 131 (e.g., all three of said CDRs); or a light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 117, SEQ ID NO: 120, and SEQ ID NO: 123 (e.g., all three of said CDRs), and/or a heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 126, SEQ ID NO: 129, and SEQ ID NO: 132 (e.g., all three of said CDRs).

In certain embodiments, the recombinant vector comprises a nucleic acid molecule, or a pair of recombinant vectors comprise nucleic acid molecules, encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin comprises a light chain comprising the CDRs of SEQ ID NO: 115, SEQ ID NO: 118 and SEQ ID NO: 121 and a heavy chain comprising the CDRs of SEQ ID NO: 124, SEQ ID NO: 127 and SEQ ID NO: 130; a light chain comprising the CDRs of SEQ ID NO: 116, SEQ ID NO: 119 and SEQ ID NO: 122 and a heavy chain comprising the CDRs of SEQ ID NO: 125, SEQ ID NO: 128 and SEQ ID NO: 131; or a light chain comprising the CDRs of SEQ ID NO: 117, SEQ ID NO: 120 and SEQ ID NO: 123 and a heavy chain comprising the CDRs of SEQ ID NO: 126, SEQ ID NO: 129 and SEQ ID NO: 132.

The one or more nucleic acids in the recombinant vector or vectors of the present invention do not encode the humanized immunoglobulin Campath®.

In other embodiments, the recombinant vector comprises a nucleic acid molecule, or a pair of recombinant vectors comprise nucleic acid molecules, encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin has a greater binding affinity for glycosylated human CD52 than for non-glycosylated or de-glycosylated human CD52, e.g., exhibits binding that is specific for glycosylated human CD52. The humanized immunoglobulin may bind to an epitope on mature human CD52 which comprises its N-linked carbohydrate moiety. This epitope may also comprise at least residue 1 of the mature human CD52 sequence, at least residue 3 of the mature human CD52 sequence, at least residues 1, 3, 4 and 5 of the mature human CD52 sequence, or at least residues 1, 2, 3, 4 and 5 of the mature human CD52 sequence.

In other embodiments, the recombinant vector comprises a nucleic acid molecule encoding a humanized light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12 or SEQ ID NO: 13, wherein the humanized light chain is not the humanized light chain of Campath®.

In other embodiments, the recombinant vector comprises a nucleic acid molecule encoding a humanized heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25, SEQ ID NO: 26, or SEQ ID NO: 137, wherein the humanized heavy chain is not the humanized heavy chain of Campath®.

In other embodiments, the recombinant vector comprises a nucleic acid molecule encoding a humanized light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 115, SEQ ID NO: 118, and SEQ ID NO: 121 (e.g., all three of said CDRs); a humanized light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 116, SEQ ID NO: 119, and SEQ ID NO: 122 (e.g., all three of said CDRs); or a humanized light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 117, SEQ ID NO: 120, and SEQ ID NO: 123 (e.g., all three of said CDRs), wherein the humanized light chain is not the humanized light chain of Campath®.

In other embodiments, the recombinant vector comprises a nucleic acid molecule encoding a humanized heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 124, SEQ ID NO: 127, and SEQ ID NO: 130 (e.g., all three of said CDRs); a humanized heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 125, SEQ ID NO: 128, and SEQ ID NO: 131 (e.g., all three of said CDRs); or a humanized heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 126, SEQ ID NO: 129, and SEQ ID NO: 132 (e.g., all three of said CDRs), wherein the humanized heavy chain is not the humanized heavy chain of Campath®.

In particular embodiments, the recombinant vector of the invention is an expression vector, such as a mammalian cell expression vector. In certain embodiments, the vector is a plasmid or a viral vector (e.g., an adenoviral or AAV vector).

The invention also relates to a host cell that comprises a (one or more) nucleic acid (e.g., recombinant) encoding a humanized immunoglobulin (humanized light chain and humanized heavy chain), a humanized light chain or a humanized heavy chain of the invention. In some embodiments, the host cell comprises a recombinant vector (e.g., expression vector, including mammalian cell expression vectors) of the invention.

In a particular embodiment, the host cell comprises a nucleic acid (one or more nucleic acids) encoding a humanized light chain and a humanized heavy chain, wherein the humanized light chain and the humanized heavy chain associate together to form a humanized immunoglobulin that has binding specificity for human CD52 and wherein the humanized immunoglobulin comprises a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 3 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 16; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 4 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 17; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 5 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 18; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 6 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 19; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 7 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 20; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 8 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 21; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 9 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 22; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 10 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 23; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 11 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 24; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 12 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 25; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 12 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 137; or a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 13 and a heavy chain sequence comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 26.

In some embodiments, the host cell comprises one or more nucleic acid molecules encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin binds to the same epitope on human CD52 as a mouse monoclonal antibody comprising a light chain variable region of SEQ ID NO: 3 and a heavy chain variable region of SEQ ID NO: 16; a light chain variable region of SEQ ID NO: 4 and a heavy chain variable region of SEQ ID NO: 17; a light chain variable region of SEQ ID NO: 5 and a heavy chain variable region of SEQ ID NO: 18; a light chain variable region of SEQ ID NO: 6 and a heavy chain variable region of SEQ ID NO: 19; a light chain variable region of SEQ ID NO: 7 and a heavy chain variable region of SEQ ID NO: 20; a light chain variable region of SEQ ID NO: 8 and a heavy chain variable region of SEQ ID NO: 21; a light chain variable region of SEQ ID NO: 9 and a heavy chain variable region of SEQ ID NO: 22; a light chain variable region of SEQ ID NO: 10 and a heavy chain variable region of SEQ ID NO: 23; a light chain variable region of SEQ ID NO: 11 and a heavy chain variable region of SEQ ID NO: 24; a light chain variable region of SEQ ID NO: 12 and a heavy chain variable region of SEQ ID NO: 25; or a light chain variable region of SEQ ID NO: 13 and a heavy chain variable region of SEQ ID NO: 26. In other embodiments, the host cell comprises one or more nucleic acid molecules encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin binds to an epitope on human CD52 which overlaps with the epitope to which such a mouse monoclonal antibody binds.

In other embodiments, the host cell comprises one or more nucleic acid molecules encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin binds to an epitope comprising at least residue 1 of mature human CD52; binds to an epitope comprising at least residues 1, 3, 4 and 5 of mature human CD52; binds to an epitope comprising at least residues 1, 2, 3, 4 and 5 of mature human CD52; or binds to an epitope comprising at least residues 7, 8 and 9 of mature human CD52. In some embodiments, the epitope comprises at least residues 7, 8 and 11 of the mature human CD52 sequence. In some embodiments, the epitope comprises at least residues 4 and 11 of the mature human CD52 sequence.

In some embodiments, the host cell comprises one or more nucleic acid molecules encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin comprises a light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 115, SEQ ID NO: 118, and SEQ ID NO: 121 (e.g., all three of said CDRs), and/or a heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 124, SEQ ID NO: 127, and SEQ ID NO: 130 (e.g., all three of said CDRs); a light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 116, SEQ ID NO: 119, and SEQ ID NO: 122 (e.g., all three of said CDRs), and/or a heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 125, SEQ ID NO: 128, and SEQ ID NO: 131 (e.g., all three of said CDRs); or a light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 117, SEQ ID NO: 120, and SEQ ID NO: 123 (e.g., all three of said CDRs), and/or a heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 126, SEQ ID NO: 129, and SEQ ID NO: 132 (e.g., all three of said CDRs).

In some embodiments, the host cell comprises one or more nucleic acid molecules encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin comprises a light chain comprising the CDRs of SEQ ID NO: 115, SEQ ID NO: 118 and SEQ ID NO: 121 and a heavy chain comprising the CDRs of SEQ ID NO: 124, SEQ ID NO: 127 and SEQ ID NO: 130; a light chain comprising the CDRs of SEQ ID NO: 116, SEQ ID NO: 119 and SEQ ID NO: 122 and a heavy chain comprising the CDRs of SEQ ID NO: 125, SEQ ID NO: 128 and SEQ ID NO: 131; or a light chain comprising the CDRs of SEQ ID NO: 117, SEQ ID NO: 120 and SEQ ID NO: 123 and a heavy chain comprising the CDRs of SEQ ID NO: 126, SEQ ID NO: 129 and SEQ ID NO: 132.

In other embodiments, the host cell comprises one or more nucleic acid molecules encoding a humanized heavy chain and a humanized light chain which associate together to form a humanized immunoglobulin that has binding specificity for human CD52, wherein the humanized immunoglobulin has a greater binding affinity for glycosylated human CD52 than for non-glycosylated or de-glycosylated human CD52, e.g., exhibits binding that is specific for glycosylated human CD52. The humanized immunoglobulin may bind to an epitope on mature human CD52 which comprises its N-linked carbohydrate moiety. This epitope may also comprise at least residue 1 of the mature human CD52 sequence, at least residue 3 of the mature human CD52 sequence, at least residues 1, 3, 4 and 5 of the mature human CD52 sequence, or at least residues 1, 2, 3, 4 and 5 of the mature human CD52 sequence.

In some embodiments, the host cell comprises a nucleic acid molecule encoding a humanized light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12 or SEQ ID NO: 13. The humanized light chain is not the humanized light chain of Campath®.

In other embodiments, the host cell comprises a nucleic acid molecule encoding a humanized heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25, SEQ ID NO: 26, or SEQ ID NO: 137. The humanized heavy chain is not the humanized heavy chain of Campath®.

In some embodiments, the host cell comprises a nucleic acid encoding a humanized light chain, wherein the humanized light chain comprises one or more CDRs selected from the group consisting of SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 29, SEQ ID NO: 30, SEQ ID NO: 31, SEQ ID NO: 32, SEQ ID NO: 33, SEQ ID NO: 34, SEQ ID NO: 35, SEQ ID NO: 36, SEQ ID NO: 37, SEQ ID NO: 38, SEQ ID NO: 39, SEQ ID NO: 40, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43, SEQ ID NO: 44, SEQ ID NO: 45, SEQ ID NO: 46, SEQ ID NO: 47, and SEQ ID NO: 48 or a combination thereof, wherein the humanized light chain is not the humanized light chain of Campath®.

In other embodiments, the host cell comprises a nucleic acid encoding a humanized heavy chain, wherein the humanized heavy chain comprises one or more CDRs selected from the group consisting of SEQ ID NO: 49, SEQ ID NO: 50, SEQ ID NO: 51, SEQ ID NO: 52, SEQ ID NO: 53, SEQ ID NO: 54, SEQ ID NO: 55, SEQ ID NO: 56, SEQ ID NO: 57, SEQ ID NO: 58, SEQ ID NO: 59, SEQ ID NO: 60, SEQ ID NO: 61, SEQ ID NO: 62, SEQ ID NO: 63, SEQ ID NO: 64, SEQ ID NO: 65, SEQ ID NO: 66, SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO: 69, SEQ ID NO: 70, SEQ ID NO: 71, SEQ ID NO: 72, SEQ ID NO: 73, SEQ ID NO: 74, and SEQ ID NO: 294, or a combination thereof, wherein the humanized heavy chain is not the humanized heavy chain of Campath®.

The invention also relates to a method of preparing a humanized immunoglobulin that has binding specificity for human CD52 comprising maintaining a host cell of the invention (e.g., a host cell that contains one or more recombinant nucleic acids that encode a humanized immunoglobulin of the invention (e.g., a humanized light chain and a humanized heavy chain of the invention)) under conditions appropriate for expression of a humanized immunoglobulin, whereby humanized immunoglobulin chains are expressed and a humanized immunoglobulin is produced. In some embodiments, the method further comprises purifying or isolating the humanized immunoglobulin. In some embodiments, the method further comprises combining the purified or isolated humanized immunoglobulin with a physiologically acceptable vehicle or carrier to produce a pharmaceutical composition.

The invention also relates to a method of preparing a humanized light chain that has binding specificity for human CD52 comprising maintaining a host cell of the invention (e.g., a host cell that contains one or more recombinant nucleic acids that encode a humanized light chain of the invention) under conditions appropriate for expression of a humanized light chain, whereby a humanized light chain is expressed and a humanized light chain is produced. In some embodiments, the method further comprises purifying or isolating the humanized light chain.

The invention also relates to a method of preparing a humanized heavy chain that has binding specificity for human CD52 comprising maintaining a host cell of the invention (e.g., a host cell that contains one or more recombinant nucleic acids that encode a humanized heavy chain of the invention) under conditions appropriate for expression of a humanized heavy chain, whereby a humanized heavy chain is expressed and a humanized heavy chain is produced. In some embodiments, the method further comprises purifying or isolating the humanized heavy chain.

The invention further relates to a pharmaceutical composition comprising a humanized immunoglobulin of the invention (e.g., comprising a humanized light chain of the invention and/or a humanized heavy chain of the invention) and a physiologically acceptable vehicle or carrier. In some embodiments, the pharmaceutical composition comprises a unit dose composition.

The invention also relates to a method of producing a hybridoma that secretes a monoclonal antibody that has binding specificity for human CD52 comprising administering lymphocytes of a mouse transgenic for human CD52 to a non-transgenic mouse of the same, or of a similar, strain (e.g., CD1) as the human CD52 transgenic mouse, thereby producing an immunized, non-transgenic mouse. Splenocytes of the immunized, non-transgenic mouse are fused with immortalized cells, thereby producing a hybridoma. The hybridoma is maintained under conditions in which it will secrete a monoclonal antibody having binding specificity for human CD52. In some embodiments, FACS analysis is used to detect a hybridoma that secretes a monoclonal antibody that has binding specificity for human CD52. In other embodiments, the strain of the transgenic mouse and the strain of the non-transgenic mouse are identical. In certain embodiments, the CD52 is wildtype human CD52. In some embodiments, the CD52 transgenic mouse and the non-transgenic mouse are CD1 mice. In some embodiments, the lymphocytes used for immunization are obtained from the spleen of the human CD52 transgenic mouse. In some embodiments, the immortalized cells are selected from the group consisting of SP2/0 Ag14 cells and NS1 myeloma cells. The invention also relates to a hybridoma produced by the methods of the invention. Optionally, the monoclonal antibody secreted by the hybridoma is collected and can be further purified (e.g., substantially purified, isolated). In other embodiments, the method further comprises determining the nucleotide sequence of the monoclonal antibody secreted by the hybridoma.

The invention also relates to a method for treating an autoimmune disease (e.g., multiple sclerosis (MS), rheumatoid arthritis (RA) (See e.g., Nature Reviews Drug Discovery 6: 75-92 (2007)), vasculitis (See e.g., Rheumatology 39:229-237 (2000)), Behcet's disease (BD) (See e.g., Rheumatology 42:1539-1544 (2003)), lupus and celiac disease (Vivas, S., et al., N Engl. J. Med., 354(23):2514-2515 (2006)), vasculitis, psoriasis, myositis, scleroderma, aplastic anemia, and colitis) in a patient in need thereof, comprising administering to the patient an effective amount of a humanized immunoglobulin of the invention.

In another aspect, an effective amount of a humanized immunoglobulin of the invention can be administered in conjunction with one or more immunosuppressive agents to prepare a patient in need thereof for a solid organ transplant (Agarwal et al., Transplant Immunol., 20:6-11 (2008)) or a CD34+ stem cell transplant (Burt et al., The Lancet, published online Jan. 30, 2009).

The invention also relates to a method for treating cancer in a patient in need thereof, comprising administering to the patient an effective amount of a humanized immunoglobulin of the invention.

The invention also relates to a method for treating multiple sclerosis in a patient in need thereof, comprising administering to the patient an effective amount of a humanized immunoglobulin of the invention.

The invention also relates to a method for treating chronic lymphocytic leukemia in a patient in need thereof, comprising administering to the patient an effective amount of a humanized immunoglobulin of the invention.

The administration of a humanized immunoglobulin of the present invention may comprise the administration of the humanized immunoglobulin per se (e.g., in a pharmaceutical composition), the administration of one or more recombinant vectors encoding the humanized immunoglobulin, or the administration of a host cell which comprises one or more nucleic acids (e.g., one or more recombinant vectors) encoding the humanized immunoglobulins and expresses the humanized immunoglobulin.

The invention also relates to a method of diagnosing a disease selected from the group consisting of autoimmune diseases (e.g., multiple sclerosis, lupus, vasculitis), cancer (e.g., leukemias (e.g., chronic lymphocytic leukemia), and lymphomas (e.g., non-Hodgkin's lymphoma)), transplant (e.g., solid organ transplant (e.g., kidney transplant) and stem cell transplant), ‘comprising assaying a patient sample in vitro with a humanized immunoglobulin of the invention.

The invention also relates to a humanized immunoglobulin of the invention (e.g., comprising a humanized light chain of the invention and/or humanized heavy chain of the invention), a recombinant vector of the invention, or a host cell of the invention, for use in medicine, such as for use in therapy and/or diagnosis of a disease such as for use in treating a disease or disorder described herein such as an autoimmune disease (e.g., multiple sclerosis, rheumatoid arthritis, and lupus), cancer, a lymphocyte hyper-proliferative condition (e.g., T or B cell malignancies including leukemia such as B-cell chronic lymphocytic leukemia and lymphomas such as non-Hodgkin's lymphoma). See, e.g., Lundin, J., et al., Blood, 101:4267-4272 (2003); Rodig, S J., et al., Clinical Cancer Research, 12(23):7174-7179 (2006). The invention also relates to the use of a humanized immunoglobulin, humanized light chain or humanized heavy chain of the invention, a recombinant vector of the invention, or a host cell of the invention, for the manufacture of a medicament for treating a disease or disorder described herein (e.g., autoimmune diseases (e.g., multiple sclerosis, lupus, vasculitis), cancer (e.g., leukemias (e.g., chronic lymphocytic leukemia), and lymphomas (e.g., non-Hodgkin's lymphoma)), and transplant (e.g., solid organ transplant (e.g., kidney transplant) and stem cell transplant)').

The invention further provides humanized anti-human CD52 antibodies comprising human light chain framework regions that utilize a human Vk2-A18b gene in which residues 36 (Y) and 46 (L) (Kabat numbering) have been substituted. In some embodiments, residue 36 is V or L and residue 46 is R. The invention also provides humanized anti-human CD52 antibodies comprising human heavy chain framework regions that utilize a human VH 3-23 gene in which residue 47 (W) (Kabat numbering) has been substituted. In some embodiments, residues 47 (W) and 49 (S) (Kabat numbering) both have been substituted. In some embodiments, residue 47 is L and residue 49 is S. In other embodiments, residue 47 is L and residue 49 is A.

In some embodiments, a humanized anti-human CD52 antibody of the invention has an EC₅₀ value as determined in a cell-binding assay such as the assay described in Example 29 that is two-fold lower than the EC₅₀ value for Campath-1H® antibody. In various embodiments, the humanized anti-human CD52 antibody has an EC₅₀ value of 11 nM or less.

In some embodiments, a humanized anti-human CD52 antibody of the invention binds CD52 on cells in the presence of anti-Campath-1H® antibodies from the serum of a human patient who has been treated with Campath-1H®. That is, the binding of a humanized anti-human CD52 antibody of the invention to CD52 on cells is not reduced in the presence of such anti-Campath-1H® antibodies compared to Campath-1H® binding to CD52 or is less reduced in the presence of such anti-Campath-1H® antibodies compared to Campath-1H® binding to CD52.

The invention further provides humanized anti-human CD52 antibodies with a lymphocyte depletion profile in blood and/or spleen of a humanized anti-human CD52 antibody provided herein.

In some embodiments, a humanized anti-human CD52 antibody of the invention increases the circulating level of one or more of TNFalpha, IL-6 and MCP-1 in the serum of a subject.

In some embodiments, a humanized anti-human CD52 antibody of the invention reduces lymphocyte levels in a subject for at least 30 days, at least 50 days, at least 60 days, at least 70 days, at least 80 days or for more than 80 days.

In some embodiments, a humanized anti-human CD52 antibody of the invention delays the onset of disease and/or decreases the severity of disease as measured by clinical score in a mouse EAE model.

In some embodiments, a humanized anti-human CD52 antibody of the invention is less immunogenic than Campath-1H® in an immunogenicity assay such as the assay described in Example 69 or 70.

Mouse Monoclonal Immunoglobulins

The invention also relates to mouse monoclonal antibodies (mouse monoclonal immunoglobulins) that have binding specificity for human CD52. In one embodiment, the invention relates to a mouse monoclonal antibody that has binding specificity for human CD52, comprising a light chain comprising SEQ ID NO: 3 and a heavy chain comprising SEQ ID NO: 16; a light chain comprising SEQ ID NO: 4 and a heavy chain comprising SEQ ID NO: 17; a light chain comprising SEQ ID NO: 5 and a heavy chain comprising SEQ ID NO: 18; a light chain comprising SEQ ID NO: 6 and a heavy chain comprising SEQ ID NO: 19; a light chain comprising SEQ ID NO: 7 and a heavy chain comprising SEQ ID NO: 20; a light chain comprising SEQ ID NO: 8 and a heavy chain comprising SEQ ID NO: 21; a light chain comprising SEQ ID NO: 9 and a heavy chain comprising SEQ ID NO: 22; a light chain comprising SEQ ID NO: 10 and a heavy chain comprising SEQ ID NO: 23; a light chain comprising SEQ ID NO: 11 and a heavy chain comprising SEQ ID NO: 24; a light chain comprising SEQ ID NO: 12 and a heavy chain comprising SEQ ID NO: 25; or a light chain comprising SEQ ID NO: 13 and a heavy chain comprising SEQ ID NO: 26.

In one embodiment, the mouse monoclonal antibody that has binding specificity for human CD52 comprises a light chain variable region selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, and SEQ ID NO: 13, or a heavy chain variable region selected from the group consisting of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25, and SEQ ID NO: 26, or both such light chain variable region and such heavy chain variable region.

The invention also relates to a mouse immunoglobulin light chain comprising the variable region of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12 or SEQ ID NO: 13.

The invention also relates to a mouse immunoglobulin heavy chain comprising the variable region of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25 or SEQ ID NO: 26.

Preferably, the mouse monoclonal antibodies of the present invention comprise both a mouse antibody light chain of the invention and a mouse antibody heavy chain of the invention. In some embodiments, the invention provides a mouse monoclonal immunoglobulin which binds to the same epitope on human CD52 as a mouse monoclonal antibody comprising a light chain variable region of SEQ ID NO: 3 and a heavy chain variable region of SEQ ID NO: 16; a light chain variable region of SEQ ID NO: 4 and a heavy chain variable region of SEQ ID NO: 17; a light chain variable region of SEQ ID NO: 5 and a heavy chain variable region of SEQ ID NO: 18; a light chain variable region of SEQ ID NO: 6 and a heavy chain variable region of SEQ ID NO: 19; a light chain variable region of SEQ ID NO: 7 and a heavy chain variable region of SEQ ID NO: 20; a light chain variable region of SEQ ID NO: 8 and a heavy chain variable region of SEQ ID NO: 21; a light chain variable region of SEQ ID NO: 9 and a heavy chain variable region of SEQ ID NO: 22; a light chain variable region of SEQ ID NO: 10 and a heavy chain variable region of SEQ ID NO: 23; a light chain variable region of SEQ ID NO: 11 and a heavy chain variable region of SEQ ID NO: 24; a light chain variable region of SEQ ID NO: 12 and a heavy chain variable region of SEQ ID NO: 25; or a light chain variable region of SEQ ID NO: 13 and a heavy chain variable region of SEQ ID NO: 26. In other embodiments, the invention provides a mouse monoclonal immunoglobulin which binds to an epitope on human CD52 which overlaps with the epitope to which such a mouse monoclonal antibody binds.

In other embodiments, the invention provides a mouse monoclonal immunoglobulin which binds to an epitope on human CD52 comprising at least residue 1 of the mature human CD52 sequence. The mouse monoclonal immunoglobulin may bind to an epitope comprising at least residues 1, 3, 4 and 5 of the mature human CD52 sequence, may bind to an epitope comprising at least residues 1, 2, 3, 4 and 5 of the mature human CD52 sequence, or may bind to an epitope comprising at least residues 7, 8 and 9 of the mature human CD52 sequence. In some embodiments, the epitope comprises at least residues 7, 8 and 11 of the mature human CD52 sequence. In some embodiments, the epitope comprises at least residues 4 and 11 of the mature human CD52 sequence.

The invention also relates to isolated nucleic acid molecules that encode the mouse monoclonal immunoglobulins, mouse immunoglobulin light chains or mouse immunoglobulin heavy chains of the invention. In some embodiments, the invention is an isolated nucleic acid molecule encoding a mouse immunoglobulin heavy chain and a mouse immunoglobulin light chain which associate together to form a mouse monoclonal immunoglobulin that has binding specificity for human CD52, wherein the mouse immunoglobulin light chain comprises a variable region selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12 and SEQ ID NO: 13, or the mouse immunoglobulin heavy chain comprises a variable region selected from the group consisting of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25 and SEQ ID NO: 26, or both such light chain and such heavy chain.

In some embodiments, the isolated nucleic acid encodes a mouse immunoglobulin light chain which comprises a variable region selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, and SEQ ID NO: 13.

In other embodiments, the isolated nucleic acid encodes a mouse immunoglobulin heavy chain which comprises a variable region selected from the group consisting of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25, and SEQ ID NO: 26.

The invention also relates to recombinant vectors (e.g., expression vectors, including mammalian cell expression vectors) that comprise a nucleic acid encoding the mouse monoclonal immunoglobulin (e.g., a mouse immunoglobulin light chain and a mouse immunoglobulin heavy chain), the mouse immunoglobulin light chain, or the mouse immunoglobulin heavy chain of the invention. In some embodiments, the invention is a recombinant vector comprising a nucleic acid, or a pair of recombinant vectors comprising nucleic acids encoding a mouse monoclonal immunoglobulin that comprises a light chain variable region selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12 and SEQ ID NO: 13, or a heavy chain variable region selected from the group consisting of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25, and SEQ ID NO: 26, or both such light chain variable region and heavy chain variable region.

In other embodiments, the recombinant vector comprises a nucleic acid encoding a mouse immunoglobulin light chain, wherein the mouse immunoglobulin light chain comprises SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12 or SEQ ID NO: 13.

In other embodiments, the recombinant vector comprises a nucleic acid encoding a mouse immunoglobulin heavy chain, wherein the mouse immunoglobulin heavy chain comprises SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25 or SEQ ID NO: 26.

In other embodiments, the recombinant vector comprises a nucleic acid encoding a mouse immunoglobulin light chain and a mouse immunoglobulin heavy chain, wherein the mouse immunoglobulin light chain and mouse immunoglobulin heavy chain associate together to form a mouse monoclonal immunoglobulin that has binding specificity for human CD52. In one embodiment, the mouse immunoglobulin light chain comprises a variable region selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12 and SEQ ID NO: 13, and the mouse immunoglobulin heavy chain comprises a variable region selected from the group consisting of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25, and SEQ ID NO: 26.

In particular embodiments, the recombinant vector of the invention is an expression vector, such as a mammalian cell expression vector. In certain embodiments, the vector is a plasmid or a viral vector (e.g., an adenoviral or AAV vector).

The invention also relates to a host cell that comprises one or more nucleic acids encoding the mouse monoclonal immunoglobulin (mouse immunoglobulin light chain and mouse immunoglobulin heavy chain), the mouse immunoglobulin light chain or the mouse immunoglobulin heavy chain of the invention. For example, in some embodiments, the host cell comprises a recombinant vector (e.g., expression vector, mammalian cell expression vector) of the invention.

In some embodiments, the host cell comprises nucleic acid encoding a mouse immunoglobulin light chain and a mouse immunoglobulin heavy chain, wherein the mouse immunoglobulin light chain and the mouse immunoglobulin heavy chain associate together to form a mouse monoclonal immunoglobulin that has binding specificity for human CD52 and wherein the mouse immunoglobulin light chain comprises a variable region selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12 and SEQ ID NO: 13, and/or the mouse immunoglobulin heavy chain comprises a varaiable region selected from the group consisting of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25 and SEQ ID NO: 26, or both.

In some embodiments, the host cell comprises nucleic acid encoding a mouse immunoglobulin light chain, wherein the mouse immunoglobulin light chain comprises a light chain variable region selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12 and SEQ ID NO: 13.

In some embodiments, the host cell comprises a nucleic acid encoding a mouse immunoglobulin heavy chain, wherein the mouse immunoglobulin heavy chain comprises a heavy chain variable region selected from the group consisting of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25 and SEQ ID NO: 26.

The invention also relates to a method of preparing a mouse monoclonal immunoglobulin comprising maintaining a host cell of the invention (e.g., a host cell that contains one or more recombinant nucleic acids (e.g., recombinant vectors) that encode a mouse monoclonal immunoglobulin (e.g., a mouse immunoglobulin light chain and a mouse immunoglobulin heavy chain) of the invention) under conditions appropriate for expression of a mouse monoclonal immunoglobulin, whereby mouse monoclonal immunoglobulin chains are expressed and a mouse monoclonal immunoglobulin is produced. In some embodiments, the method further comprises purifying or isolating the mouse monoclonal immunoglobulin.

The invention also relates to a method of preparing a light chain of a mouse monoclonal immunoglobulin, comprising maintaining a host cell of the invention containing a nucleic acid encoding a mouse immunoglobulin light chain of the invention under conditions appropriate for expression of said mouse immunoglobulin light chain, whereby a light chain is expressed. In some embodiments, the method further comprises purifying or isolating the light chain.

The invention also relates to a method of preparing a heavy chain of a mouse monoclonal immunoglobulin, comprising maintaining a host cell of the invention containing a nucleic acid encoding a mouse immunoglobulin heavy chain of the invention under conditions appropriate for expression of said mouse immunoglobulin heavy chain, whereby a mouse immunoglobulin heavy chain is expressed. In some embodiments, the method further comprises purifying or isolating the mouse immunoglobulin heavy chain.

The invention also relates to a method of diagnosing a disease (e.g., autoimmune diseases (e.g., multiple sclerosis, lupus, vasculitis), cancer (e.g., leukemias (e.g., chronic lymphocytic leukemia), and lymphomas (e.g., non-Hodgkin's lymphoma)), and transplant (e.g., solid organ transplant (e.g., kidney transplant) and stem cell transplant)′) comprising assaying a patient sample in vitro, with the mouse monoclonal immunoglobulin of the invention (e.g., Lundin, J., et al., Blood, 101:4267-4272 (2003); Rodig, S J, et al., Clin. Cancer res., 12(23); 7174-717179 (2006)).

Chimeric Immunoglobulins

The invention also relates to chimeric immunoglobulins that have binding specificity for human CD52. Such chimeric immunoglobulins may include the variable regions of any of the mouse monoclonal immunoglobulin of the present invention. In one embodiment, the chimeric immunoglobulin of the invention comprises the light chain variable region of SEQ ID NO: 3 and the heavy chain variable region of SEQ ID NO: 16; the light chain variable region of SEQ ID NO: 4 and the heavy chain variable region of SEQ ID NO: 17; the light chain variable region of SEQ ID NO: 5 and the heavy chain variable region of SEQ ID NO: 18; the light chain variable region of SEQ ID NO: 6 and the heavy chain variable region of SEQ ID NO: 19; the light chain variable region of SEQ ID NO: 7 and the heavy chain variable region of SEQ ID NO: 20; the light chain variable region of SEQ ID NO: 8 and the heavy chain variable region of SEQ ID NO: 21; the light chain variable region of SEQ ID NO: 9 and the heavy chain variable region of SEQ ID NO: 22; the light chain variable region of SEQ ID NO: 10 and the heavy chain variable region of SEQ ID NO: 23; the light chain variable region of SEQ ID NO: 11 and the heavy chain variable region of SEQ ID NO: 24; the light chain variable region of SEQ ID NO: 12 and the heavy chain variable region of SEQ ID NO: 25; or the light chain variable region of SEQ ID NO: 13 and the heavy chain variable region of SEQ ID NO: 26.

The invention also relates to a chimeric antibody that has binding specificity for human CD52, comprising a light chain variable region sequence selected from the group consisting of: the light chain variable region of SEQ ID NO: 3, the light chain variable region of SEQ ID NO: 4, the light chain variable region of SEQ ID NO: 5, the light chain variable region of SEQ ID NO: 6, the light chain variable region of SEQ ID NO: 7, the light chain variable region of SEQ ID NO: 8, the light chain variable region of SEQ ID NO: 9, the light chain variable region of SEQ ID NO: 10, the light chain variable region of SEQ ID NO: 11, the light chain variable region of SEQ ID NO: 12 and the light chain variable region of SEQ ID NO: 13, and/or a heavy chain variable region sequence selected from the group consisting of: the heavy chain variable region of SEQ ID NO: 16, the heavy chain variable region of SEQ ID NO: 17, the heavy chain variable region of SEQ ID NO: 18, the heavy chain variable region of SEQ ID NO: 19, the heavy chain variable region of SEQ ID NO: 20, the heavy chain variable region of SEQ ID NO: 21, the heavy chain variable region of SEQ ID NO: 22, the heavy chain variable region of SEQ ID NO: 23, the heavy chain variable region of SEQ ID NO: 24, the heavy chain variable region of SEQ ID NO: 25 and the heavy chain variable region of SEQ ID NO: 26.

The invention also relates to a chimeric light chain comprising a variable region selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, and SEQ ID NO: 13.

The invention also relates to a chimeric heavy chain comprising a variable region selected from the group consisting of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25, and SEQ ID NO: 26.

Preferably, the chimeric immunoglobulins of the present invention comprise both a chimeric light chain of the invention and a chimeric heavy chain of the invention.

In some embodiments, the invention provides a chimeric immunoglobulin which binds to the same epitope on human CD52 as a mouse monoclonal antibody comprising a light chain variable region of SEQ ID NO: 3 and a heavy chain variable region of SEQ ID NO: 16; a light chain variable region of SEQ ID NO: 4 and a heavy chain variable region of SEQ ID NO: 17; a light chain variable region of SEQ ID NO: 5 and a heavy chain variable region of SEQ ID NO: 18; a light chain variable region of SEQ ID NO: 6 and a heavy chain variable region of SEQ ID NO: 19; a light chain variable region of SEQ ID NO: 7 and a heavy chain variable region of SEQ ID NO: 20; a light chain variable region of SEQ ID NO: 8 and a heavy chain variable region of SEQ ID NO: 21; a light chain variable region of SEQ ID NO: 9 and a heavy chain variable region of SEQ ID NO: 22; a light chain variable region of SEQ ID NO: 10 and a heavy chain variable region of SEQ ID NO: 23; a light chain variable region of SEQ ID NO: 11 and a heavy chain variable region of SEQ ID NO: 24; a light chain variable region of SEQ ID NO: 12 and a heavy chain variable region of SEQ ID NO: 25; or a light chain variable region of SEQ ID NO: 13 and a heavy chain variable region of SEQ ID NO: 26. In other embodiments, the chimeric immunoglobulin binds to an epitope on human CD52 which overlaps with the epitope to which such a mouse monoclonal antibody binds.

In other embodiments, the invention provides a chimeric immunoglobulin which binds to an epitope on human CD52 comprising at least residue 1 of the mature human CD52 sequence. The chimeric immunoglobulin may bind to an epitope comprising at least residues 1, 3, 4 and 5 of the mature human CD52 sequence, may bind to an epitope comprising at least residues 1, 2, 3, 4 and 5 of the mature human CD52 sequence, or may bind to an epitope on human CD52 comprising at least residues 7, 8 and 9 of the mature human CD52 sequence. In some embodiments, the epitope comprises at least residues 7, 8 and 11 of the mature human CD52 sequence. In some embodiments, the epitope comprises at least residues 4 and 11 of the mature human CD52 sequence.

The invention also relates to isolated nucleic acid molecules that encode the chimeric immunoglobulins, chimeric light chains or chimeric heavy chains of the invention. In some embodiments, the invention is an isolated nucleic acid molecule (one or more nucleic acid molecules) encoding a chimeric heavy chain and a chimeric light chain which associate together to form a chimeric immunoglobulin that has binding specificity for human CD52, wherein the chimeric light chain comprises a variable region selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, and SEQ ID NO: 13; and/or the chimeric heavy chain comprises a variable region selected from the group consisting of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25 and SEQ ID NO: 26.

In some embodiments, the invention is an isolated nucleic acid molecule encoding a chimeric light chain that comprises the variable region of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12 or SEQ ID NO: 13.

In some embodiments, the invention is an isolated nucleic acid molecule encoding a chimeric heavy chain that comprises the variable region of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25 or SEQ ID NO: 26.

The invention also relates to recombinant vectors (e.g., expression vectors, mammalian cell expression vectors) that comprise a nucleic acid encoding the chimeric immunoglobulin (chimeric light chain and chimeric heavy chain), the chimeric light chain, or the chimeric heavy chain of the invention. In some embodiments, the invention is a recombinant vector comprising a nucleic acid (or a pair of recombinant vectors comprising nucleic acids) encoding a chimeric immunoglobulin that comprises a light chain variable region selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12 and SEQ ID NO: 13; or a heavy chain variable region selected from the group consisting of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25, and SEQ ID NO: 26; or both such light chain and heavy chain.

In other embodiments, the recombinant vector comprises a nucleic acid encoding a chimeric light chain, wherein the chimeric light chain comprises the variable region of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12 or SEQ ID NO: 13.

In other embodiments, the recombinant vector comprises a nucleic acid encoding a chimeric heavy chain, wherein the chimeric heavy chain comprises the variable region of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25 or SEQ ID NO: 26.

In particular embodiments, the recombinant vector of the invention is an expression vector, such as a mammalian cell expression vector. In certain embodiments, the vector is a plasmid or a viral vector (e.g., an adenoviral or AAV vector).

The invention also relates to a host cell that comprises one or more nucleic acids (e.g., one or more recombinant vectors) encoding the chimeric immunoglobulin (chimeric light chain and chimeric heavy chain), the chimeric light chain or the chimeric heavy chain of the invention. For example, in some embodiments, the host cell comprises a recombinant vector (e.g., expression vector, mammalian cell expression vector) of the invention.

In some embodiments, the host cell comprises a recombinant nucleic acid (or a pair of recombinant nucleic acids) encoding a chimeric light chain and a chimeric heavy chain, wherein the chimeric light chain and the chimeric heavy chain associate together to form a chimeric immunoglobulin that has binding specificity for human CD52 and wherein the chimeric light chain comprises a variable region selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12 and SEQ ID NO: 13; and/or the chimeric heavy chain comprises a variable region selected from the group consisting of the variable region of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25 and SEQ ID NO: 26.

In some embodiments, the host cell comprises a recombinant nucleic acid encoding a chimeric light chain, wherein the chimeric light chain comprises a light chain variable region selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, and SEQ ID NO: 13.

In some embodiments, the host cell comprises a recombinant nucleic acid encoding a chimeric heavy chain, wherein the chimeric heavy chain comprises a heavy chain variable region selected from the group consisting of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25 and SEQ ID NO: 26.

The invention also relates to a method of preparing a chimeric immunoglobulin comprising maintaining a host cell of the invention (e.g., a host cell that contains one or more isolated nucleic acids that encode a chimeric immunoglobulin (e.g., a chimeric light chain and a chimeric heavy chain) of the invention) under conditions appropriate for expression of a chimeric immunoglobulin, whereby chimeric immunoglobulin chains are expressed and a chimeric immunoglobulin is produced. In some embodiments, the method further comprises purifying or isolating the chimeric immunoglobulin.

The invention also relates to a method of preparing a chimeric light chain comprising maintaining a host cell of the invention (e.g., a host cell that contains a nucleic acid encoding a chimeric light chain of the invention) under conditions appropriate for expression of said chimeric light chain, whereby a chimeric light chain is expressed and a chimeric light chain is produced. In some embodiments, the method further comprises purifying or isolating the chimeric light chain.

The invention also relates to a method of preparing a chimeric heavy chain comprising maintaining a host cell of the invention (e.g., a host cell that contains a nucleic acid encoding a chimeric heavy chain of the invention) under conditions appropriate for expression of said chimeric heavy chain, whereby a chimeric heavy chain is expressed and a chimeric heavy chain is produced. In some embodiments, the method further comprises purifying or isolating the chimeric heavy chain.

The invention also relates to a method of diagnosing a disease selected from the group consisting of autoimmune diseases (e.g., multiple sclerosis, lupus, vasculitis), cancer (e.g., leukemias (e.g., chronic lymphocytic leukemia), and lymphomas (e.g., non-Hodgkin's lymphoma)), and transplant (e.g., solid organ transplant (e.g., kidney transplant) and stem cell transplant', comprising assaying a patient sample in vitro, with the chimeric immunoglobulin of the invention.

Further embodiments of this invention are described as follows. In one aspect, the invention relates to a monoclonal anti-human CD52 antibody or an antigen-binding portion thereof, wherein the light chain and heavy chain of said antibody comprise the three complementarity determining regions (CDRs) found in: SEQ ID NOs: 3 and 16, respectively; SEQ ID NOs: 4 and 17, respectively; SEQ ID NOs: 5 and 18, respectively; SEQ ID NOs: 6 and 19, respectively; SEQ ID NOs: 7 and 20, respectively; SEQ ID NOs: 8 and 21, respectively; SEQ ID NOs: 9 and 22, respectively; SEQ ID NOs: 10 and 23, respectively; SEQ ID NOs: 11 and 24, respectively; SEQ ID NOs: 12 and 25, respectively; SEQ ID NOs: 12 and 137, respectively; or SEQ ID NOs: 13 and 26, respectively. In some embodiments, the invention relates to an antibody that binds to the same epitope on human CD52 as the above monoclonal antibody or antigen-binding portion. In some embodiments, the invention relates to an antibody that competes with the above monoclonal antibody or antigen-binding portion. In some embodiments, the invention relates to an antibody that cross-competes with the above monoclonal antibody or antigen-binding portion.

In some embodiments, any of the above antibodies or antigen-binding portions binds to an amino acid sequence comprising SEQ ID NO: 104. In some related embodiments, the binding of said antibody or portion to SEQ ID NO: 104 may be reduced by an alanine substitution at one or more of residues 4, 7, 8, or 11 of SEQ ID NO: 104.

In some embodiments, the antibody is a humanized antibody, a mouse antibody, or a chimeric antibody. In certain embodiments, the framework regions of the heavy chain of said antibody utilize a VH3-72 or VH3-23 human germline sequence, and the framework regions of the light chain of said antibody utilize a VK2 A18b human germline sequence.

In some embodiments, the invention relates to a monoclonal anti-human CD52 antibody or an antigen-binding portion thereof, wherein said antibody comprises heavy chain (H)-CDR1, H-CDR2, H-CDR3, and light chain (L)-CDR1, L-CDR2, and L-CDR3 whose amino acid sequences are SEQ ID NOs: 51, 59, 69, 29, 36, and 43, respectively; SEQ ID NOs: 50, 60, 69, 29, 37, and 43, respectively; SEQ ID NOs: 50, 61, 68, 29, 38, and 43, respectively; SEQ ID NOs: 50, 61, 69, 29, 36, and 43, respectively; SEQ ID NOs: 50, 62, 69, 29, 39, and 43, respectively; SEQ ID NOs: 52, 61, 70, 30, 40, and 43, respectively; SEQ ID NOs: 53, 63, 71, 31, 36, and 44, respectively; SEQ ID NOs: 54, 64, 71, 31, 36, and 45, respectively; SEQ ID NOs: 55, 63, 72, 31, 36, and 46, respectively; SEQ ID NOs: 56, 65, 73, 32, 41, and 47, respectively; SEQ ID NOs: 56, 65, 294, 32, 41, and 47, respectively; or SEQ ID NOs: 56, 66, 74, 33, 41, and 48, respectively.

In some embodiments, the invention relates to a monoclonal anti-human CD52 antibody or an antigen-binding portion thereof, wherein the light chain and heavy chain of said antibody comprise the amino acid sequences of SEQ ID NOs: 3 and 16, respectively; SEQ ID NOs: 4 and 17, respectively; SEQ ID NOs: 5 and 18, respectively; SEQ ID NOs: 6 and 19, respectively; SEQ ID NOs: 7 and 20, respectively; SEQ ID NOs: 8 and 21, respectively; SEQ ID NOs: 9 and 22, respectively; SEQ ID NOs: 10 and 23, respectively; SEQ ID NOs: 11 and 24, respectively; SEQ ID NOs: 12 and 25, respectively; or SEQ ID NOs: 13 and 26, respectively.

In some embodiments, the invention relates to a monoclonal antibody or antigen-binding portion thereof, wherein the heavy chain and light chain of said antibody comprise the amino acid sequences of SEQ ID NOs: 103 and 102, respectively; SEQ ID NOs: 136 and 138, respectively; SEQ ID NOs: 137 and 138, respectively; SEQ ID NOs: 139 and 147, respectively; SEQ ID NOs: 149 and 155, respectively; SEQ ID NOs: 149 and 156, respectively; SEQ ID NOs: 158 and 165, respectively; SEQ ID NOs: 158 and 166, respectively; SEQ ID NOs: 159 and 165, respectively; SEQ ID NOs: 159 and 166, respectively; SEQ ID NOs: 161 and 166, respectively; or SEQ ID NOs: 163 and 166, respectively. In some embodiments, the invention relates to an antibody that binds to the same epitope on human CD52 as the above monoclonal antibody or antigen-binding portion. In some embodiments, the invention relates to an antibody that competes with the above monoclonal antibody or antigen-binding portion. In some embodiments, the invention relates to an antibody that cross-competes with the above monoclonal antibody or antigen-binding portion.

In certain embodiments, the invention relates to a monoclonal humanized anti-human CD52 antibody or an antigen-binding portion thereof, wherein the heavy chain and the light chain of said antibody comprise the amino acid sequences of SEQ ID NOs: 272 and 273, respectively, without the signal sequences. In certain embodiments, the invention relates to a monoclonal anti-human CD52 antibody or an antigen-binding portion thereof, wherein the heavy chain and the light chain of said antibody comprise the amino acid sequences of SEQ ID NOs: 274 and 275, respectively, without the signal sequences. In certain embodiments, the invention relates to a monoclonal anti-human CD52 antibody or an antigen-binding portion thereof, wherein the heavy chain and the light chain of said antibody comprise the amino acid sequences of SEQ ID NOs: 276 and 278, respectively, without the signal sequences. In certain embodiments, the invention relates to a monoclonal anti-human CD52 antibody or an antigen-binding portion thereof, wherein the heavy chain and the light chain of said antibody comprise the amino acid sequences of SEQ ID NOs: 277 and 278, respectively, without the signal sequences. In certain embodiments, the invention relates to a monoclonal anti-human CD52 antibody or an antigen-binding portion thereof, wherein the heavy chain and the light chain of said antibody comprise the amino acid sequences of SEQ ID NOs: 279 and 280, respectively, without the signal sequences. In certain embodiments, the invention relates to a monoclonal anti-human CD52 antibody or an antigen-binding portion thereof, wherein the heavy chain and the light chain of said antibody comprise the amino acid sequences of SEQ ID NOs: 281 and 282, respectively, without the signal sequences. The invention also provides antibodies that bind to the same epitope on CD52 as one of these humanized antibodies and antibodies that compete or cross-compete with one of these humanized antibodies. In related embodiments, the invention provides compositions comprising one such humanized antibody and a pharmaceutically acceptable carrier.

In some embodiments, the invention relates to a monoclonal anti-human CD52 antibody or an antigen-binding portion thereof, wherein the light chain of said antibody comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 102, 138, 145-148, 153-157, and 164-168. In certain embodiments, the invention relates to a monoclonal anti-human CD52 antibody or an antigen-binding portion thereof, wherein the light chain of said antibody comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 273, 275, 278, 280, and 282, without the signal sequences. In certain embodiments, the invention relates to an antibody light chain or a portion thereof, comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 102, 138, 145-148, 153-157, 164-168, 273, 275, 278, 280, and 282, without the signal sequences if present.

In some embodiments, the invention relates to a monoclonal anti-human CD52 antibody or an antigen-binding portion thereof, wherein the heavy chain of said antibody comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 103, 136, 137, 139-144, 149-152, and 158-163. In certain embodiments, the invention relates to a monoclonal anti-human CD52 antibody or an antigen-binding portion thereof, wherein the heavy chain of said antibody comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 272, 274, 276, 277, 279, and 281, without the signal sequences. In certain embodiments, the invention relates to an antibody heavy chain or a portion thereof, comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 103, 136, 137, 139-144, 149-152, 158-163, 272, 274, 276, 277, 279, and 281, without the signal sequences if present.

In some embodiments, any of the above antibodies may be an IgG, IgM, IgA, IgD or IgE molecule. In certain embodiments, said IgG is IgG1, IgG2, IgG3, or IgG4.

In some embodiments, any of the above antigen-binding portions may be a single chain antibody, Fv, Fab, Fab′, F(ab′)2, Fd, single chain Fv molecule (scFv), bispecific single chain Fv dimer, diabody, domain-deleted antibody or single domain antibody (dAb).

The invention also relates to any of the above antibodies or antigen-binding portions, wherein said antibody or antigen-binding portion depletes T or B lymphocytes, or both; preferentially depletes T lymphocytes as compared to B lymphocytes; increases circulating serum levels of TNF-alpha, IL-6, or MCP-1 (e.g., by at least 5%, at least 10%, at least 50%, at least 100% or at least 200%); mediates antibody-dependent cell mediated cytotoxicity (ADCC) of CD52-expressing cells; mediates complement-dependent cytotoxicity (CDC) of CD52-expressing cells; binds to human CD52 in spite of the presence of neutralizing antibodies to alemtuzumab in a human patient; and/or promotes intracellular signaling in human T and/or B cells (see, e.g., Hederer et al., International Immunology 12:505-616 (2000); Watanabe et al., Clinical Immunology 120: 247-259 (2006)).

The invention further relates to an isolated nucleic acid encoding the heavy chain or an antigen-binding portion thereof, or the light chain or an antigen-binding portion thereof, of any of the above antibodies. In some embodiments, said isolated nucleic acid comprises a heavy chain nucleotide sequence selected from the group consisting of SEQ ID NOs: 283, 285, 287, 288, 290, and 292, or said nucleotide sequence without the sequence encoding a signal peptide; a light chain nucleotide sequence selected from the group consisting of SEQ ID NOs: 284, 286, 289, 291, and 293, or said nucleotide sequence without the sequence encoding a signal peptide; or both said heavy chain nucleotide sequence and said light chain nucleotide sequence. In certain embodiments, said isolated nucleic acid comprises a heavy chain nucleotide sequence and a light chain nucleotide sequence selected from the group consisting of SEQ ID NO: 283 and SEQ ID NO: 284, respectively, both without sequences encoding signal peptides; SEQ ID NO: 285 and SEQ ID NO: 286, respectively, both without sequences encoding signal peptides; SEQ ID NO: 287 and SEQ ID NO: 289, respectively, both without sequences encoding signal peptides; SEQ ID NO: 288 and SEQ ID NO: 289, respectively, both without sequences encoding signal peptides; SEQ ID NO: 290 and SEQ ID NO: 291, respectively, both without sequences encoding signal peptides; and SEQ ID NO: 292 and SEQ ID NO: 293, respectively, both without sequences encoding signal peptides.

The invention also relates to the use of an isolated nucleic acid comprising a heavy chain nucleotide sequence and an isolated nucleic acid comprising a light chain nucleotide sequence for the manufacture of a medicament for treating a patient in need thereof, wherein said heavy chain nucleotide sequence and light chain nucleotide sequence are selected from the group consisting of SEQ ID NO: 283 and SEQ ID NO: 284, respectively, both without sequences encoding signal peptides; SEQ ID NO: 285 and SEQ ID NO: 286, respectively, both without sequences encoding signal peptides; SEQ ID NO: 287 and SEQ ID NO: 289, respectively, both without sequences encoding signal peptides; SEQ ID NO: 288 and SEQ ID NO: 289, respectively, both without sequences encoding signal peptides; SEQ ID NO: 290 and SEQ ID NO: 291, both respectively, without sequences encoding signal peptides; and SEQ ID NO: 292 and SEQ ID NO: 293, both respectively, without sequences encoding signal peptides.

The invention also relates to a recombinant vector comprising (1) a nucleic acid sequence encoding the heavy chain or an antigen-binding portion thereof, (2) a nucleic acid sequence encoding the light chain or an antigen-binding portion thereof, or (3) both, of any of the above antibodies. The invention further relates to a host cell comprising a first nucleic acid sequence encoding the heavy chain or an antigen-binding portion thereof of any of the above antibodies, said first nucleic acid sequence operably linked to an expression control element, and a second nucleic acid sequence encoding the light chain or an antigen-binding portion thereof of said antibody, said second nucleic acid sequence operably linked to an expression control element. The invention relates to a method of making an anti-human CD52 antibody or an antigen-binding portion thereof, comprising maintaining said host cell under conditions appropriate for expression of the antibody or portion, and also relates to said method further comprising the step of isolating the antibody or portion.

The invention relates to a composition comprising the monoclonal antibody or antigen-binding portion according to any one of claims 1-24 and a pharmaceutically acceptable vehicle or carrier.

In some embodiments, the invention relates to a method for treating a patient in need thereof, comprising administering to the patient an effective amount of any of the above antibodies or antigen-binding portions, or the above composition. In certain embodiments, said patient is receiving a transplantation.

In some embodiments, the invention relates to a method for treating an autoimmune disease in a patient in need thereof, comprising administering to the patient an effective amount of any of the above antibodies or antigen-binding portions, or the above composition. In certain embodiments, the autoimmune disease is, e.g., multiple sclerosis, rheumatoid arthritis, or systemic lupus erythematosus.

In some embodiments, the invention relates to a method for treating cancer in a patient in need thereof, comprising administering to the patient an effective amount of any of the above antibodies or antigen-binding portions, or the above composition. In certain embodiments, the cancer is, e.g., a lymphoma such as non-Hodgkin's lymphoma; a leukemia such as B-cell chronic lymphocytic leukemia; T cell malignancy, wherein the antibody or portion preferentially depletes T cells as compared to B cells; or a solid tumor.

In some embodiments, any of the above methods of treatment further comprising administering to the patient a neutrophil or NK cell stimulatory agent. In certain embodiments, said agent is G-CSF or GM-CSF. In some embodiments, any of the above methods of treatment further comprises administering to the patient a T regulatory cell stimulatory agent. In certain embodiments, said agent is rapamycin.

In some embodiments, the invention relates to a method for inhibiting angiogenesis in a patient in need thereof, comprising administering an effective amount of any of the above antibodies or antigen-binding portions to the patient. In certain embodiments, the patient has a solid tumor. In certain embodiments, the patient has neovascularization. In certain embodiments, said neovascularization is in the eye.

The invention also relates to the use of any of the above antibodies or antigen-binding portions for the manufacture of a medicament for treating an autoimmune disease in a patient in need thereof. Further, the invention relates to the use of any of the above antibodies or antigen-binding portions for the manufacture of a medicament for treating cancer in a patient in need thereof. The invention relates to the use of any of the above antibodies or antigen-binding portions for the manufacture of a medicament for treating a patient in need of a transplantation. The invention relates to the use of any of the above antibodies or antigen-binding portions for the manufacture of a medicament for treating neovascularization in a patient in need thereof.

The invention also relates to the use of any of the above antibodies or antigen-binding portions as a medicament.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1A-1B is a schematic representation of the development of new anti-CD52 monoclonal antibodies. The general scheme is depicted in FIG. 1A and the names of the mouse anti-human CD52 antibody clones as well as their isotypes in shown in FIG. 1B.

FIG. 2 is an alignment of the amino acid sequences of several mouse anti-human CD52 kappa light chain sequences (SEQ ID NOS:1-13). Campath-1G is the rat monoclonal antibody from which the humanized Campath-1H antibody is derived.

FIG. 3 is an alignment of the amino acid sequences of several mouse anti-human CD52 heavy chain sequences (SEQ ID NOS:14-26).

FIG. 4 is an alignment of wildtype CD52 and 10 mutant CD52 proteins (SEQ ID NOS: 104-114, from top to bottom).

FIG. 5A illustrates the FACS-based N-terminal binding profile of antibodies 4B10 and 7F11 on cells expressing CD52 alanine scanning mutants.

FIG. 5B illustrates the FACS-based middle region binding profile of antibodies CF1D12, 3G7, 9D9, 5F7, 4G7, and 11C11 on cells expressing CD52 alanine scanning mutants.

FIG. 5C illustrates the FACS-based binding profile of antibodies Campath-1H® (“Campath 1H”), 2C3, 12G6, and 23E6 on cells expressing CD52 alanine scanning mutants.

FIG. 5D depicts immunoblots of CD52+/−N-linked glycosylation probed with the panel of chimeric monoclonal antibodies. “C1H” stands for Campath-1H®.

FIG. 6 is a graph showing the results of a 1.5 hour CDC assay on various chimeric anti-CD52 antibodies screened on CHO-K1 CD52 #67 cells. The results show that chimeric antibodies 4B10 and 7F11 are comparable to or better than Campath-1H® (“Campath 1H”).

FIG. 7 is a graph showing the results of a 14 hour ADCC assay on various chimeric IgG1 antibodies to CD52 screened on CHO-K1 CD52 #67 cells. The results show that chimeric antibodies 2C3 and 12G6 are comparable to or better than Campath-1H® (“Campath 1-H”).

FIG. 8A-8C illustrate the comparative binding of various anti-CD52 antibodies and the Campath-1H® (“C-1H”) antibody to defined human lymphocyte populations. These figures show the hierarchy of the binding ability of the chimeric antibodies screened by FACS assay. Curves to the far right demonstrate the highest binding ability, whereas curves to the left bind with lower affinity.

FIGS. 9A-9C are graphs illustrating the level of CD4 T cells (FIG. 9A), CD8 T cells (FIG. 9B) and CD19 B cells (FIG. 9C) in the blood 72 hours after dosing with chimeric antibodies 7F11, 8G3, 23E6, 12G6, 4B10, or 5F7, or Campath-1H® (“Cam”).

FIGS. 10A-10C are graphs illustrating the level of CD4 T cells (FIG. 10A), CD8 T cells (FIG. 10B) and CD19 B cells (FIG. 10C) in the spleen 72 hours after dosing with chimeric antibodies 7F11, 8G3, 23E6, 12G6, 4B10, or 5F7, or Campath-1H® (“Cam”).

FIGS. 11A-11C are graphs showing the level of CD4 T cells (FIG. 11A), CD8 T cells (FIG. 11B) and CD19 B cells (FIG. 11C) in the blood 72 hours after dosing with chimeric antibodies 2C3, 9D9, 4B10, 3G7, or 11C11, or Campath-1H® (“Cam”).

FIG. 12 is a Kaplan Meier Survival graph illustrating the percent of surviving mice after treatment with 7F11, 4B10, or 12G6 chimeric monoclonal antibodies, or Campath-1H® (“Campath”).

FIG. 13 is a Kaplan Meier Survival graph illustrating the percent of surviving mice after treatment with 2C3, 8G3, or 23E6 chimeric monoclonal antibodies, or Campath-1H® (“Campath”).

FIG. 14 is a Kaplan Meier Survival graph illustrating the percent of surviving mice after treatment with 9D9 or 4B10 chimeric monoclonal antibodies, or Campath-1H® (“Campath”).

FIG. 15 is a Kaplan Meier Survival graph illustrating the percent of surviving mice after treatment with 2C3 or 11C11 chimeric monoclonal antibodies, or Campath-1H® (“Campath”).

FIG. 16 is an alignment of the mouse anti-human CD52 antibody 4B10 heavy chain variable region (SEQ ID NO: 96) sequence with the closest matched human germline sequence (SEQ ID NO: 97) and the humanized heavy chain variable region sequence (SEQ ID NO: 98). Also shown is an alignment of the mouse anti-human CD52 antibody 4B10 light chain variable region (SEQ ID NO: 99) sequence with the closest matched human germline sequence (SEQ ID NO: 100) and the humanized light chain variable region sequence (SEQ ID NO: 101).

FIG. 17 shows the humanized 4B10 heavy chain (SEQ ID NO: 103) and light chain (SEQ ID NO: 102) variable region sequences.

FIG. 18 is a graph showing that humanized antibody 4B10-H1/K1 (“4B10-Humanized”) and chimeric antibody 4B10 bind equivalently to cells expressing CD52.

FIG. 19 is a graph showing that humanized antibody 4B10-H1/K1 (“4B10 Humanized”) and chimeric antibody 4B10 mediate equivalent ADCC activity on cells expressing CD52.

FIG. 20 is a graph showing that humanized antibody 4B10-H1/K1 (“4B10-Humanized”) and chimeric antibody 4B10 mediate equivalent CDC activity on cells expressing CD52.

FIG. 21 is a graph illustrating the pharmacokinetic profile of chimeric anti-CD52 antibodies (12G6, 7F11 and 4B10), Campath-1H® (“Campath”), and humanized anti-CD52 antibody 4B10-H1/K1 (“4B10 humanized (H1/K1)”) in heterozygous huCD52 transgenic mice.

FIGS. 22A-22C are graphs showing the level of CD4 T cells (FIG. 22A), CD8 T cells (FIG. 22B) and CD19 B cells (FIG. 22C) in the blood 72 hours after dosing with chimeric antibody 4B10 or humanized antibody 4B10-H1/K1 (“4B10-Hu”) or Campath-1H® (“Campath”).

FIG. 23 is a graph showing the summary of the relative binding affinities of the anti-CD52 monoclonal antibodies.

FIG. 24 shows the humanized 7F11 heavy and light (kappa) chain variable region sequences. Amino acid residues that are back mutated to mouse residues are underlined and the CDRs are shown in boldface.

FIG. 25 is a histogram showing that chimeric and humanized 7F11 antibodies bind equivalently to cells expressing CD52. The X axis represents the fluorescence emitted by the bound anti-CD52 antibody, while the area of each peak represents the total cell population.

FIG. 26A shows the humanized 2C3 heavy chain variable region sequences. Amino acid residues that are back mutated to mouse residues are underlined and the CDRs are shown in boldface. FIG. 26B shows the humanized 2C3 light (kappa) chain variable region sequences. Amino acid residues that are back mutated to mouse residues are underlined and the CDRs are shown in boldface.

FIG. 27A is a histogram showing binding of humanized and chimeric 2C3 antibodies to cells expressing CD52. The X axis represents the fluorescence emitted by the bound anti-CD52 antibody, while the area of each peak represents the total cell population. FIG. 27B is a histogram showing that chimeric and a subset of the humanized 2C3 antibodies bind equivalently to cells expressing CD52. The X axis represents the fluorescence emitted by the bound anti-CD52 antibody, while the area of each peak represents the total cell population.

FIG. 28A shows the humanized 12G6 heavy chain variable region sequences. Amino acid residues that are back mutated to mouse residues are underlined and the CDRs are shown in boldface. FIG. 28B shows the humanized 12G6 light (kappa) chain variable region sequences. Amino acid residues that are back mutated to mouse residues are underlined and the CDRs are shown in boldface.

FIG. 29 is a histogram showing that chimeric and a subset of the humanized 12G6 antibodies bind equivalently to cells expressing CD52. The X axis represents the fluorescence emitted by the bound anti-CD52 antibody, while the area of each peak represents the total cell population.

FIG. 30A shows the humanized 9D9 heavy chain variable region sequences. Amino acid residues that are back mutated to mouse residues are underlined and the CDRs are shown in boldface. FIG. 30B shows the humanized 9D9 light (kappa) chain variable region sequences. Amino acid residues that are back mutated to mouse residues are underlined and the CDRs are shown in boldface.

FIG. 31 is a histogram showing that chimeric and a subset of the humanized 9D9 antibodies bind equivalently to cells expressing CD52. The X axis represents the fluorescence emitted by the bound anti-CD52 antibody, while the area of each peak represents the total cell population.

FIG. 32A shows the binding curves of Campath-1H® (“C1H”), a chimeric 2C3 antibody, and a humanized 2C3-SFD1/K12 antibody to primary human T cells and huCD52 transgenic mouse T cells. FIG. 32B shows the binding curves of Campath-1H® (“C1H”), a chimeric 9D9 antibody, and humanized 9D9 antibodies to primary human T cells and huCD52 transgenic mouse T cells. FIG. 32C shows the binding curves of Campath-1H® (“C1H”), a chimeric 12G6 antibody, and humanized 12G6 antibodies to primary human T cells and huCD52 transgenic mouse T cells.

FIG. 33 is a table showing the relative binding efficiency of Campath-1H®, chimeric 2C3 and 12G6 antibodies, and humanized 2C3 and 12G6 antibodies to huCD52 expressing human and transgenic mouse T cells.

FIG. 34 illustrates the comparative binding patterns of humanized anti-CD52 Campath-1H®, 2C3, 12G6, and 9D9 antibodies to defined subsets of human peripheral blood mononuclear cell populations by flow cytometry. These histograms show that the humanized anti-CD52 antibody binding is equivalent to that of Campath-1H® for various CD52 expressing human PBMC subsets. The X axis represents the fluorescence emitted by the bound anti-CD52 antibody, while the area of each peak represents the total cell population.

FIG. 35 is a graph showing that chimeric and humanized 7F11 antibodies mediate equivalent ADCC activity on cells expressing CD52.

FIG. 36 is a graph showing that chimeric and humanized 7F11 antibodies mediate CDC activity on cells expressing CD52.

FIG. 37 is a graph showing that chimeric and humanized 2C3 antibodies mediate ADCC activity on cells expressing CD52.

FIG. 38 is a graph showing that chimeric and humanized 2C3 antibodies mediate CDC activity on cells expressing CD52.

FIG. 39 is a graph showing that chimeric and humanized 12G6 antibodies mediate ADCC activity on cells expressing CD52.

FIG. 40 is a graph showing that chimeric and humanized 12G6 antibodies mediate CDC activity on cells expressing CD52.

FIG. 41 is a graph showing that chimeric and humanized 9D9 antibodies mediate ADCC activity on cells expressing CD52.

FIG. 42 is a graph showing that chimeric and humanized 9D9 antibodies mediate CDC activity on cells expressing CD52.

FIG. 43 is a graph showing the ADCC activity of humanized anti-CD52 antibodies on primary T cells.

FIG. 44 is a graph showing the CDC activity of humanized anti-CD52 antibodies on primary T cells.

FIG. 45 is a graph showing neutralization of Campath-1H but not other anti-CD52 antibodies with CAMMS223 study human serum samples that contain anti-Campath-1H® neutralizing antibodies. Serum samples were taken from a representative patient (MS-1) at month 12 (M12) and month 13 (M13).

FIGS. 46A-46E show the level of CD4+ T cells, CD8+ T cells, B220+ B cells, NK cells, myeloid cells, and neutrophils in the blood 72 hours after dosing with Campath-1H® (“Campath”) and humanized 4B10-H1/K1 (“4B10”) antibodies.

FIGS. 47A-47E show the level of CD4+ T cells, CD8+ T cells, B220+ B cells, NK cells, myeloid cells, neutrophils, and macrophages in the spleen 72 hours after dosing with Campath-1H® (“Campath”) and humanized 4B10-H1/K1 (“4B10”) antibodies.

FIGS. 48A-48E show the levels of circulating cytokines 2 hours after dosing with Campath-1H® (“Campath”) and humanized 4B10-H1/K1 (“4B10”) antibodies.

FIGS. 49A and 49B show the repopulation of circulating lymphocytes over a time course after dosing with Campath-1H® (“Campath”) and humanized 4B10-H1/K1 (“4B10”) antibodies, (mg/kg).

FIGS. 50A-50E show the level of CD4+ T cells, CD8+ T cells, B220+ B cells, NK cells, myeloid cells, and neutrophils in the blood 72 hours after dosing with the humanized 7F11-SFD1/K2 (“7F11 SFD1”) and 7F11-SFD2/K2 (“7F11 SFD2”) antibodies.

FIGS. 51A-51E show the level of CD4+ T cells, CD8+ T cells, B220+ B cells, NK cells, myeloid cells, and neutrophils in the spleen 72 hours after dosing with the humanized 7F11-SFD1/K2 (“7F11 SFD1”) and 7F11-SFD2/K2 (“7F11 SFD2”) antibodies.

FIGS. 52A-52F show the levels of circulating cytokines 2 hours after dosing with the humanized 7F11-SFD1/K2 (“7F11 SFD1”) and 7F11-SFD2/K2 (“7F11 SFD2”) antibodies.

FIGS. 53A and 53B show the repopulation of circulating lymphocytes over a timecourse after dosing with the humanized 7F11-SFD1/K2 (“7F11 SFD1”) and 7F11-SFD2/K2 (“7F11 SFD2”) antibodies, (mg/kg).

FIGS. 54A and 54B show the level of CD4+ T cells, CD8+ T cells and B220+ B cells in the blood 72 hours after dosing with Campath-1H® (“Campath”), 7F11-chimeric antibodies, and humanized 7F11-SFD1/K2 and 7F11-SFD2/K2 antibodies.

FIG. 55 shows the level of Campath-1H® (“Campath”), 7F11-chimeric antibody and humanized 7F11-SFD1/K2 and 7F11-SFD2/K2 antibodies in the blood over a timecourse after dosing.

FIGS. 56A-56E show the level of CD4+ T cells, CD8+ T cells, B220+ B cells, NK cells, and neutrophils in the blood 72 hours after dosing with 2C3-SFD1/K12 antibodies.

FIGS. 57A-57E show the level of CD4+ T cells, CD8+ T cells, B220+ B cells, NK cells, and neutrophils in the spleen 72 hours after dosing with 2C3-SFD1/K12 antibodies.

FIGS. 58A-58F show the levels of circulating cytokines 2 hours after dosing with 2C3-SFD1/K12 (“2C3”) antibodies.

FIG. 59 shows the repopulation of circulating lymphocytes over a timecourse after dosing with 2C3-SFD1/K12 antibodies, (mg/kg).

FIGS. 60A-60E show the level of CD4+ T cells, CD8+ T cells, B220+ B cells, NK cells, myeloid cells, macrophages, and neutrophils in the blood 72 hours after dosing with 12G6-SFD1/K11 antibodies.

FIGS. 61A-61E show the level of CD4+ T cells, CD8+ T cells, B220+ B cells, NK cells, macrophages, neutrophils, and myeloid cells in the spleen 72 hours after dosing with 12G6-SFD1/K11 antibodies.

FIGS. 62A-62F show the levels of circulating cytokines 2 hours after dosing with 12G6-SFD1/K11 (“12G6 hu”) antibodies.

FIG. 63 shows the repopulation of circulating lymphocytes over a timecourse after dosing with 12G6-SFD1/K11 antibodies, (mg/kg).

FIGS. 64A-64C show the level of 2C3-chimeric, 2C3-SFD1/K12, 12G6-chimeric, 12G6-SFD1/K11, 9D9-chimeric, and 9D9-H10/K12 antibodies in the blood over a timecourse after dosing.

FIGS. 65A-65E show the level of CD4+ T cells, CD8+ T cells, B220+ B cells, NK cells, myeloid cells, macrophages, and neutrophils in the blood 72 hours after dosing with 9D9-H10/K12 (“9D9”) antibodies.

FIGS. 66A-66E show the level of CD4+ T cells, CD8+ T cells, B220+ B cells, NK cells, myeloid cells, neutrophils, and macrophages in the spleen 72 hours after dosing with 9D9-H10/K12 (“9D9”) antibodies.

FIGS. 67A-67F show the levels of circulating cytokines 2 hours after dosing with 9D9-H10/K12 (“9D9”) antibodies.

FIG. 68 shows the repopulation of circulating lymphocytes over a timecourse after dosing with 9D9-H10/K12 (“9D9”) antibodies, (mg/kg).

FIGS. 69A-69D show the level of bulk lymphocyte populations (CD4+ T cells, CD8+ T cells, and B cells) and CD4+ T cell, CD8+ T cell, B220+ B cell and NK cell subtypes in the blood 72 hours after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12 (“2C3”), 12G6-SFD1/K11 (“12G6”), and 9D9-H10/K12 (“9D9”) antibodies.

FIGS. 70A-70D show the level of bulk lymphocyte populations (CD4+ T cells, CD8+ T cells, and B cells) and CD4+ T cell, CD8+ T cell, B220+ B cell and NK cell subtypes in the spleen 72 hours after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12 (“2C3”), 12G6-SFD1/K11 (“12G6”), and 9D9-H10/K12 (“9D9”) antibodies.

FIGS. 71A-71F show the levels of circulating cytokines 2 hours after dosing with Campath-1H®, 2C3-SFD1/K12, 12G6-SFD1/K11, and 9D9-H10/K12 antibodies.

FIG. 72 shows the level of CD4+ T cells, CD8+ T cells, B220+ B cells, and NK cells in the blood 72 hours after dosing with 9D9-H10/K12 and 9D9-H11/K12 antibodies.

FIG. 73 shows the level of CD4+ T cells, CD8+ T cells, B220+ B cells, and NK cells in the spleen 72 hours after dosing with 9D9-H10/K12 and 9D9-H11/K12 antibodies.

FIGS. 74A-74D show the level of CD4+ T cells, CD8+ T cells, B220+ B cells, NK cells, and myeloid cells in the blood 72 hours after dosing with 12G6-SFD1/K11 (“12G6 K11”) and 12G6-SFD1/K12 (“12G6 K12”) antibodies.

FIGS. 75A-75D show the level of CD4+ T cells, CD8+ T cells, B220+ B cells, NK cells and myeloid cells in the spleen 72 hours after dosing with 12G6-SFD1/K11 (“12G6 K11”) and 12G6-SFD1/K12 (“12G6 K12”) antibodies.

FIG. 76 shows the level of bulk lymphocyte populations (CD4+ T cells, CD8+ T cells, and B220+ B cells) in the blood 72 hours after dosing with 9D9-H11/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies.

FIGS. 77A-77D show the level of CD4+ T cell, CD8+ T cell, B220+ B cell, NK cell, and myeloid cell subtypes in the blood 72 hours after dosing with 9D9-H11/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies.

FIG. 78 shows the level of bulk lymphocyte populations (CD4+ T cells, CD8+ T cells, and B220+ B cells) in the spleen 72 hours after dosing with 9D9-H11/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies.

FIGS. 79A-79D show the level of CD4+ T cell, CD8+ T cell, B220+ B cell, NK cell, and myeloid cell subtypes in the spleen 72 hours after dosing with 9D9-H11/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies.

FIGS. 80A-80F show the levels of circulating cytokines 2 hours after dosing with 9D9-H11/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies.

FIGS. 81A and 81B show the level of 2C3-SFD1/K12, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13 and 9D9-H18/K13 antibodies in the blood over a timecourse after dosing.

FIGS. 82A-82F show the level of cytokines in the blood over a 48-hour timecourse following dosing with Campath-1H® (“Campath”), 2C3-SFD1/K11, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13 or 9D9-H18/K13 antibodies.

FIGS. 83A-83E show the level of bulk lymphocytes, CD4+ T cells, CD8+ T cells, B220+ B cells, NK cells, and myeloid cells in the spleen 72 hours after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K11, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13 or 9D9-H18/K13 antibodies.

FIGS. 84A-84G show the repopulation of circulating CD4+ and CD8+ T cells, regulatory T cells, B cells, NK cells, neutrophils and macrophages over a timecourse after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12 antibodies.

FIG. 85 shows the ability of FITC-labeled Campath-1H® (“Campath”), 2C3-SFD1/K12 (“2C3 K12”), 12G6-SFD1/K11 (“12G6 K11”), 12G6-SFD1/K12 (“12G6 K12”), 9D9-H16/K13 (“9D9 H16”), and 9D9-H18/K13 (“9D9 H18”) antibodies to specifically bind huCD52 lymphocyte cell populations in the spleen.

FIGS. 86A-86E show the level of bulk lymphocyte populations (CD4+ T cells, CD8+ T cells, and B220+ B cells) and CD4+ T cell, CD8+ T cell, B220+ B cell, NK cell, and myeloid cell subtypes in the blood 72 hours after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies.

FIGS. 87A-87E show the level of bulk lymphocyte populations (CD4+ T cells, CD8+ T cells, and B220+ B cells) and CD4+ T cell, CD8+ T cell, B220+ B cell, NK cell, and myeloid cell subtypes in the spleen 72 hours after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies.

FIGS. 88A-88F show the levels of circulating cytokines 2 hours after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies.

FIGS. 89A-89D show the level of CD4+ T cell, CD8+ T cell, B220+ B cell, and NK/myeloid cell subtypes in the blood 72 hours after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12 antibodies.

FIGS. 90A-90D show the level of CD4+ T cell, CD8+ T cell, B220+ B cell, and NK/myeloid cell subtypes in the spleen 72 hours after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12 antibodies.

FIGS. 91A-91D show the level of CD4+ T cell, CD8+ T cell, B220+ B cell, and NK/myeloid cell subtypes in the lymph node 72 hours after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12 antibodies.

FIG. 92A shows the huCD52 expression level on CD4+ T cell, CD8+ T cell, B220+ B cell, and NK/myeloid cell subtypes in huCD52-KI/KO and non-transgenic control mice. FIG. 92B shows the huCD52 expression level on CD4+ T cells, CD8+ T cells, and B cells in huCD52-KI/KO and huCD52 CD1 transgenic mice.

FIG. 93 shows the binding to huCD52 of 12G6-SFD1/K12 and 2C3-SFD1/K12 antibodies from various production sources (“small scale” and “large scale”) as compared to a Campath-1H® control.

FIG. 94 shows the level of bulk lymphocyte populations (CD4+ T cells, CD8+ T cells, B220+ B cells and NK cells) in the blood 72 hours after dosing with 12G6-SFD1/K12 and 2C3-SFD1/K12 antibodies from various production sources (“small scale” and “large scale”).

FIG. 95 shows the levels of 2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12 antibodies in the blood over a timecourse after dosing.

FIG. 96 demonstrates the EAE clinical score of 2C3-SFD1/K12 and 12G6-SFD1/K12 over a timecourse of disease progression.

FIGS. 97A and 97B demonstrate the ability of Campath1H® (“Campath”), 2C3-SFD1/K12 (“2C3”), His435Ala 2C3-SFD1/K12 (“H435A 2C3”) and His310A1a/His435Gln 2C3-SFD1/K12 (“H310A/H435Q 2C3”) to bind to mouse and human FcRn molecules.

FIG. 98 shows the in vivo clearance of 2C3-SFD1/K12 (“2C3 unmodified”), 2C3-SFD1/K12-Modified 1 (“2C3-Fc mutant 1”) and 2C3-SFD1/K12-Modified 2 (“2C3-Fc mutant 2”) in nontransgenic mice.

FIG. 99 shows the in vivo clearance of 2C3-SFD1/K12 (“2C3”), 2C3-SFD1/K12-Modified 1 (“2C3-Fc mutant 1”) and 2C3-SFD1/K12-Modified 2 (“2C3-Fc mutant 2”) in huCD52 transgenic mice.

FIGS. 100A and 100B show the level of bulk lymphocyte populations (CD4+ T cells, CD8+ T cells, B220+ B cells, and NK cells) in the blood and spleen 72 hours after dosing with 2C3-SFD1/K12 (“2C3”), 2C3-SFD1/K12-Modified 1 (“2C3 Fc mutant-1”), and 2C3-SFD1/K12-Modified 2 (“2C3 Fc mutant-2”) antibodies.

FIGS. 101A and 101B are representative sensorgrams of Biacore T100 assays to determine the epitope specificity of the humanized 12G6-SFD1/K12 antibody and mutant peptides generated by alanine scanning. FIG. 101A shows no binding between 12G6-SFD1/K12 and the MUT 8 peptide, while FIG. 101B shows binding between 12G6-SFD1/K12 and the MUT 9 peptide.

FIG. 102 shows the TCR V beta analysis for donor BMS486. CD4+ T cells educated with Campath-1H® peptide group 986-989 exhibited preferential expansion of a single V beta (Vβ3).

FIG. 103 shows the TCR V beta analysis for donor BMS928. CD4+ T cells educated with 12G6-SFD1/K12 peptide groups 1066-67-68 and 1083-84-85 exhibited preferential expansion of a single V beta (Vβ20).

FIGS. 104A-104J show the Campath-1H® immunogenicity assessment. Proliferative responses are shown in CPM for individual donors A-J. The X axis depicts the groups of peptides used to stimulate autologous CD4+ T cells three times. Each group of T cells was assayed in triplicate with autologous DCs pulsed with the educating antigen/peptide group (specific response, left bar, white), irrelevant DR binding peptide (middle bar, striped), or media (right bar, black).

FIGS. 105A-105J show the 12G6-SFD1/K12 immunogenicity assessment. Proliferative responses are shown in CPM for individual donors A-J. The X axis depicts the groups of peptides used to stimulate autologous CD4+ T cells three times. Each group of T cells was assayed in triplicate with autologous DCs pulsed with the educating peptide group (specific response, left bar, white), irrelevant DR binding peptide (middle bar, striped), or media (right bar, black). In groups assayed without the media control, the left bar (white) represents DCs pulsed with the educating peptide, and the right bar (striped) represents DCs pulsed with the irrelevant peptide.

FIG. 106 shows the full-length humanized heavy chain amino acid sequence of 2C3-SFD1 (SEQ ID NO: 272) and the full-length humanized light chain amino acid sequence of 2C3-K12 (SEQ ID NO: 273). The signal sequences are boldfaced and italicized and the CDRs are underlined.

FIG. 107 shows the full-length humanized heavy chain amino acid sequence of 7F11-SFD1 (SEQ ID NO: 274) and the full-length humanized light chain amino acid sequence of 7F11-K2 (SEQ ID NO: 275). The signal sequences are boldfaced and italicized and the CDRs are underlined.

FIG. 108 shows the full-length humanized heavy chain amino acid sequences of 9D9-H16 (SEQ ID NO: 276) and 9D9-H18 (SEQ ID NO: 277), and the full-length humanized light chain amino acid sequence of 9D9-K13 (SEQ ID NO: 278). The signal sequences are boldfaced and italicized and the CDRs are underlined.

FIG. 109 shows the full-length humanized heavy chain amino acid sequence of 12G6-SFD1 (SEQ ID NO: 279) and the full-length humanized light chain amino acid sequence of 12G6-K12 (SEQ ID NO: 280). The signal sequences are boldfaced and italicized and the CDRs are underlined.

FIG. 110 shows the full-length humanized heavy chain amino acid sequence of 4B10-H1 (SEQ ID NO: 281) and the full-length humanized light chain amino acid sequence of 4B10-K1 (SEQ ID NO: 282). The signal sequences are boldfaced and italicized and the CDRs are underlined.

FIG. 111 shows the full-length humanized heavy chain nucleic acid sequence of 2C3-SFD1 (SEQ ID NO: 283) and the full-length humanized light chain nucleic acid sequence of 2C3-K12 (SEQ ID NO: 284). The signal sequences are underlined, the variable domains are in boldface, and the constant regions are italicized.

FIG. 112 shows the full-length humanized heavy chain nucleic acid sequence of 7F11-SFD1 (SEQ ID NO: 285) and the full-length humanized light chain nucleic acid sequence of 7F11-K2 (SEQ ID NO: 286). The signal sequences are underlined, the variable domains are in boldface, and the constant regions are italicized.

FIG. 113 shows the full-length humanized heavy chain nucleic acid sequences of 9D9-H16 (SEQ ID NO: 287) and 9D9-H18 (SEQ ID NO: 288). The signal sequences are underlined, the variable domains are in boldface, and the constant regions are italicized.

FIG. 114 shows the full-length humanized light chain nucleic acid sequence of 9D9-K13 (SEQ ID NO: 289). The signal sequence is underlined, the variable domain is in boldface, and the constant region is italicized.

FIG. 115 shows the full-length humanized heavy chain nucleic acid sequence of 12G6-SFD1 (SEQ ID NO: 290) and the full-length humanized light chain nucleic acid sequence of 12G6-K12 (SEQ ID NO: 291). The signal sequences are underlined, the variable domains are in boldface, and the constant regions are italicized.

FIG. 116 shows the full-length humanized heavy chain nucleic acid sequence of 4B10-H1 (SEQ ID NO: 292) and the full-length humanized light chain nucleic acid sequence of 4B10-K1 (SEQ ID NO: 293). The signal sequences are underlined, the variable domains are in boldface, and the constant regions are italicized.

DETAILED DESCRIPTION OF THE INVENTION

CD52 is a glycosylated, GPI anchored cell surface abundant protein (approximately 5×10⁵ antibody binding sites per cell) present on at least 95% of all human peripheral blood lymphocytes and monocytes/macrophages (Hale G, et al., “The CAMPATH-1 antigen (CD52),” Tissue Antigens, 35:178-327 (1990)), but is absent from hematopoietic stem cells. This invention is directed to immunoglobulins (anti-CD52) which have binding specificity (e.g., epitopic specificity) for, or are selective for binding to, human CD52 or a portion thereof. These immunoglobulins bind specifically to a CD52, and do not bind specifically to non-CD52 molecules. Specific binding between an anti-CD52 immunoglobulin and CD52 can be determined, for example, by measuring EC₅₀ of the immunoglobulin's binding to CD52+ cells by flow cytometry. Specific binding can be indicated by an EC₅₀ range of, e.g., 0.5-10 μg/ml. The immunoglobulins described herein can have binding specificity for all or a portion of a human CD52 wherein the human CD52 is an isolated and/or recombinant human CD52, or on the surface of a cell which expresses human CD52. In addition, the immunoglobulins can have binding specificity for one or more forms of human CD52 (e.g., glycosylated human CD52; de-glycosylated human CD52; non-glycosylated human CD52; and allelic variants). In one embodiment, the immunoglobulins have binding specificity for a naturally occurring, endogenous or wildtype human CD52. The amino acid sequence of a wildtype human CD52 is set out in FIG. 4 (SEQ ID NO: 104).

The immunoglobulins described herein can be purified or isolated using known techniques. Immunoglobulins that are “purified” or “isolated” have been separated away from molecules (e.g., peptides) of their source of origin (e.g., the supernatant of cells; in a mixture such as in a mixture of immunoglobulins in a library), and include immunoglobulins obtained by methods described herein or other suitable methods. Isolated immunoglobulins include substantially pure (essentially pure) immunoglobulins, and immunoglobulins produced by chemical synthesis, recombinant techniques and a combination thereof.

More specifically, the invention relates to anti-human CD52 immunoglobulins, antigen-binding fragments (i.e., portions) of the immunoglobulins, the light chains of the immunoglobulins, the heavy chains of the immunoglobulins, and fragments of these light chains or heavy chains. The invention also relates to mature immunoglobulins or chains thereof, such as glycosylated immunoglobulins. The invention also relates to immature or precursor immunoglobulin (protein). The invention also relates to nucleic acid molecules (e.g., vectors) that encode both these immature or mature proteins, to vectors and host cells that comprise such nucleic acid, to methods of producing immature and mature proteins and to methods of using the immunoglobulins.

The immunoglobulins of this invention can be used to treat a subject in need thereof (e.g., a human patient) to deplete the subject's lymphocytes and other CD52+ cells (e.g., CD52+ cancerous cells) as needed. As used herein, “lymphocyte depletion” is a type of immunosuppression by reducing the population of circulating lymphocytes, e.g., T cells and/or

B cells, resulting in lymphopenia. The immunoglobulins of this invention can also be used to inhibit angiogenesis as further described below. The immunoglobulins of this invention also can be used to enrich hematopoietic stem cells, for example, in ex vivo applications (see, e.g., Lim et al., J. Hematology & Oncology 1:19 (2008)).

Naturally occurring immunoglobulins have a common core structure in which two identical light chains (about 24 kD) and two identical heavy chains (about 55 or 70 kD) form a tetramer. The amino-terminal portion of each chain is known as the variable (V) region and can be distinguished from the more conserved constant (C) regions of the remainder of each chain. Within the variable region of the light chain (also called the V_(L) domain) is a C-terminal portion known as the J region. Within the variable region of the heavy chain (also called the VII domain), there is a D region in addition to the J region. Most of the amino acid sequence variation in immunoglobulins is confined to three separate locations in the V regions known as hypervariable regions or complementarity determining regions (CDRs) which are directly involved in antigen binding. Proceeding from the amino-terminus, these regions are designated CDR1, CDR2 and CDR3, respectively. The CDRs are held in place by more conserved framework regions (FRs). Proceeding from the amino-terminus, these regions are designated FR1, FR2, FR3 and FR4, respectively. The locations of CDR and FR regions and a numbering system have been defined by Kabat et al. (Kabat, E. A., et al., Sequences of Proteins of Immunological Interest, Fifth Edition, U.S. Department of Health and Human Services, U.S. Government Printing Office (1991), Chothia & Lesk, Canonical Structures for the Hypervariable Regions of Immunoglobulins, J. Mol. Biol., 196, 901-917 (1987), and the IMGT® numbering system (The International ImMunoGeneTics linformation Ssystem®, Lefranc, M.-P., The Immunologist 7, 132-136 (1999). Visual inspection and sequence analysis can be carried out to identify the CDR boundaries. For this invention, the CDR sequences are defined by using both the Kabat system and the IMGT system; that is, when the CDRs defined by the two systems do not entirely overlap, we include all the residues from the sequences defined by both systems.

Human immunoglobulins can be divided into classes and subclasses, depending on the isotype of the heavy chain. The classes include IgG, IgM, IgA, IgD and IgE, in which the heavy chains are of the gamma (γ), mu (μ), alpha (α), delta (δ) or epsilon (ε) type, respectively. Subclasses include IgG1, IgG2, IgG3, IgG4, IgA1 and IgA2, in which the heavy chains are of the γ1, γ2, γ3, γ4, α1 and α2 type, respectively. Human immunoglobulin molecules of a selected class or subclass may contain either a kappa (κ) or lambda (λ) light chain. See e.g., Cellular and Molecular Immunology, Wonsiewicz, M. J., Ed., Chapter 45, pp. 41-50, W. B. Saunders Co., Philadelphia, Pa. 91991); Nisonoff, A., Introduction to Molecular Immunology, 2^(nd) Ed., Chapter 4, pp. 45-65, Sinauer Associates, Inc., Sunderland, Mass. (1984).

As used herein, the terms “immunoglobulin” and “antibody,” which are used interchangeably, refer to whole antibodies and antigen-binding fragments (i.e., “antigen-binding portions”—the two terms are used interchangeably herein unless otherwise indicated). Antigen-binding fragments of antibodies can be in the format of, for example, single chain antibodies, Fv fragments, Fab fragments, Fab′ fragments, F(ab′)2 fragments, Fd fragments, single chain Fv molecules (scFv), bispecific single chain Fv dimers (PCT/US92/09665), diabodies, domain-deleted antibodies and single domain antibodies (dAbs). See e.g., Nature Biotechnology 22(9):1161-1165 (2004)). Also within the invention are antigen-binding molecules comprising a VH and/or a VL. In the case of a VH, the molecule may also comprise one or more of a CHL hinge, CH2 and CH3 region. Such single chain antibodies are also intended to be encompassed within the term “antigen-binding portion” of an antibody.

Antibody portion or fragments can be produced by enzymatic cleavage or by recombinant techniques. For instance, papain or pepsin cleavage can be used to generate Fab or F(ab′)2 fragments, respectively. Antibodies can also be produced in a variety of truncated forms using antibody genes in which one or more stop codons have been introduced upstream of the natural stop site. For example, a recombinant construct encoding the heavy chain of an F(ab′)2 fragment can be designed to include DNA sequences encoding the CH₁ domain and hinge region of the heavy chain. Preferred antigen-binding fragments have binding specificity for a wildtype human CD52.

In another aspect, the invention provides a variant of an antibody or portion thereof as described herein, wherein said variant binds to human CD52 specifically but differs from the reference antibody or portion thereof by 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 amino acid substitutions (for example, in a CDR region, a FR region, or a constain domain). For example, the variant antibody is at least 90%, at least 91%, at least 93%, at least 95%, at least 97% or at least 99% identical to the reference antibody in the heavy chain, the heavy chain variable domain, the light chain, or the light chain variable domain.

Sequence similarity or identity for polypeptides, which is also referred to as sequence identity, is typically measured using sequence analysis software. Protein analysis software matches similar sequences using measures of similarity assigned to various substitutions, deletions and other modifications, including conservative amino acid substitutions. For instance, GCG contains programs such as “Gap” and “Bestfit” which can be used with default parameters to determine sequence homology or sequence identity between closely related polypeptides, such as homologous polypeptides from different species of organisms or between a wild type protein and a mutein thereof. See, e.g., GCG Version 6.1. Polypeptide sequences also can be compared using FASTA using default or recommended parameters, a program in GCG Version 6.1. FASTA (e.g., FASTA2 and FASTA3) provides alignments and percent sequence identity of the regions of the best overlap between the query and search sequences (Pearson, Methods Enzymol. 183:63-98 (1990); Pearson, Methods Mol. Biol. 132:185-219 (2000)). Another preferred algorithm when comparing a sequence of the invention to a database containing a large number of sequences from different organisms is the computer program BLAST, especially blastp or tblastn, using default parameters. See, e.g., Altschul et al., J. Mol. Biol. 215:403-410 (1990); Altschul et al., Nucleic Acids Res. 25:3389-402 (1997); herein incorporated by reference.

According to the invention, one type of amino acid substitution that may be made is to change one or more cysteines in the antibody, which may be chemically reactive, to another residue, such as, without limitation, alanine or serine. In one embodiment, there is a substitution of a non-canonical cysteine. The substitution can be made in a CDR or framework region of a variable domain or in the constant domain of an antibody. In some embodiments, the cysteine is canonical. Another type of amino acid substitution that may be made is to remove potential proteolytic sites in the antibody. Such sites may occur in a CDR or framework region of a variable domain or in the constant domain of an antibody. Substitution of cysteine residues and removal of proteolytic sites may decrease the risk of heterogeneity in the antibody product and thus increase its homogeneity. Another type of amino acid substitution is to eliminate asparagine-glycine pairs, which form potential deamidation sites, by altering one or both of the residues. In another aspect of the invention, the antibody may be deimmunized to reduce its immunogenicity using the techniques described in, e.g., PCT Publication WO98/52976 and WO00/34317.

Another type of amino acid substitution that may be made in one of the variants according to the invention is a conservative amino acid substitution. A “conservative amino acid substitution” is one in which an amino acid residue is substituted by another amino acid residue having a side chain R group) with similar chemical properties (e.g., charge or hydrophobicity). In general, a conservative amino acid substitution will not substantially change the functional properties of a protein. In cases where two or more amino acid sequences differ from each other by conservative substitutions, the percent sequence identity or degree of similarity may be adjusted upwards to correct for the conservative nature of the substitution. Means for making this adjustment are well-known to those of skill in the art. See e.g., Pearson, Methods Mol. Biol. 243:307-31 (1994).

Examples of groups of amino acids that have side chains with similar chemical properties include 1) aliphatic side chains: glycine, alanine, valine, leucine, and isoleucine; 2) aliphatic-hydroxyl side chains: serine and threonine; 3) amide-containing side chains: asparagine and glutamine; 4) aromatic side chains: phenylalanine, tyrosine, and tryptophan; 5) basic side chains: lysine, arginine, and histidine; 6) acidic side chains: aspartic acid and glutamic acid; and 7) sulfur-containing side chains: cysteine and methionine. Preferred conservative amino acids substitution groups are: valine-leucine-isoleucine, phenylalanine-tyrosine, lysine-arginine, alanine-valine, glutamate-aspartate, and asparagine-glutamine. Alternatively, a conservative replacement is any change having a positive value in the PAM250 log-likelihood matrix disclosed in Gonnet et al., Science 256:1443-45 (1992). A “moderately conservative” replacement is any change having a nonnegative value in the PAM250 log-likelihood matrix.

In certain embodiments, amino acid substitutions to an antibody or antigen-binding portion of the invention are those which: (1) reduce susceptibility to proteolysis, (2) reduce susceptibility to oxidation, (3) alter binding affinity for forming protein complexes, for example, to enhance ADCC and CDC activity of the antibody, (4) confer or modify other physicochemical or functional properties of such analogs, but still retain specific binding to human CD52, (5) remove C-terminal lysine, and (6) add or remove glycosylation sites.

In an aspect, the invention provides a new and novel polypeptide that is the heavy or light chain of an antibody of this invention, or that is a variable domain-containing portion of the heavy or light chain. Such a polypeptide is useful because it can partner with an opposite (light or heavy) antibody chain to form a CD52-binding molecule.

Humanized Immunoglobulins

Described herein are humanized immunoglobulins comprising the CDRs of novel mouse anti-human CD52 antibodies. In one embodiment, the humanized immunoglobulin comprises a humanized light chain and a humanized heavy chain that have CDR amino acid sequences which differ from the amino acid sequence of other humanized versions of anti-CD52 antibodies (e.g., Campath®).

The term “humanized immunoglobulin” as used herein refers to an immunoglobulin comprising chains that comprise one or more light chain CDRs (CDR1, CDR2 and CDR3) and one or more heavy chain CDRs (CDR1, CDR2 and CDR3) of an anti-CD52 antibody of non-human origin, also referred to herein as the donor antibody (e.g., a murine anti-CD52 antibody), and at least a portion of an immunoglobulin of human origin (e.g., framework regions, or framework and constant regions, derived from a light and/or heavy chain of human origin, such as CDR-grafted antibodies with or without framework changes). The humanized immunoglobulin of the invention comprises at least one CDR that differs from at least one CDR (e.g., from the corresponding CDR) present in Campath®. See, e.g., Cabilly et al., U.S. Pat. No. 4,816,567; Cabilly et al., European Patent No. 0,125,023 B1; Boss et al., U.S. Pat. No. 4,816,397; Boss et al., European Patent No. 0,120,694 B1; Neuberger, M. S. et al., WO 86/01533; Neuberger, M. S. et al., European Patent No. 0,194,276 B1; Winter, U.S. Pat. No. 5,225,539; Winter, European Patent No. 0,239,400 B1; Padlan, E. A. et al., European Patent Application No. 0,519,596 A1. See also, Ladner et al., U.S. Pat. No. 4,946,778; Huston, U.S. Pat. No. 5,476,786; and Bird, R. E. et al., Science, 242: 423-426 (1988)), regarding single chain antibodies. In some embodiments, humanized immunoglobulins are de-immunized antibodies. See, e.g., Carr et al., U.S. Pat. No. 7,264,806, regarding de-immunized immunoglobulins that have been modified to reduce the number of potential T-cell epitopes, thereby reducing the propensity for the immunoglobulin to elicit an immune response upon administration to a human.

In particular embodiments, the humanized immunoglobulin comprises one or more light chain CDRs and one or more heavy chain CDRs of one or more of the following murine monoclonal antibodies: mouse 8G3.25.3.5, mouse 4G7.F3, mouse 9D9. A2, mouse 11C11.C5, mouse 3G7.E9, mouse 5F7.1.1.4, mouse 12G6.15.1.2, mouse 23E6.2.2.1, mouse 2C3.3.8.1, mouse 7F11.1.9.7, and mouse 4B10.1.2.4.

In another embodiment, the humanized immunoglobulins bind human CD52 with an affinity similar to or better than that of Campath®. In a particular embodiment, the humanized immunoglobulin of the present invention has the binding specificity of a murine anti-human CD52 antibody of the invention (e.g., having specificity for human CD52, having the same or similar epitopic specificity) and/or it has the same inhibitory function. The humanized immunoglobulins can have the binding specificity and/or inhibitory activity of a murine anti-human CD52 antibody or humanized anti-human CD52 antibody described herein, and/or the epitopic specificity of a murine anti-human CD52 antibody or humanized anti-human CD52 antibody described herein (e.g., it can compete with the murine anti-human CD52 antibody, or another humanized anti-CD52 antibody (e.g., Campath®) for binding to CD52, and/or it can have the inhibitory function of the murine or humanized anti-human CD52 antibody). In a particular embodiment, the humanized immunoglobulin has the binding specificity, epitopic specificity and/or inhibitory activity of any one of mouse antibodies 8G3, 4G7, 9D9, 11C11, 3G7, 5F7, 12G6, 23E6, 2C3, 7F11, andr 4B10.

The portion of the humanized immunoglobulin or immunoglobulin chain which is of human origin (e.g., framework region; constant region) can be derived from any suitable human immunoglobulin or immunoglobulin chain. For example, a human constant region or portion thereof in a humanized or chimeric antibody can be derived from a human κ or λ light chain gene, and/or from a human γ (e.g., γ1, γ2, γ3, γ4), a (e.g., α1, α2), δ or ε heavy chain gene, including allelic variants. A particular constant region (e.g., IgG1), variant or portion thereof can be selected in order to tailor effector function. For example, a mutated constant region (variant) can be incorporated into the immunoglobulin or immunoglobulin chain so as to minimize binding to Fc receptors and/or ability to fix complement. (See e.g., Winter et al., GB 2,209,757 B; Morrison et al., WO 89/07142; Morgan et al., WO 94/29351, Dec. 22, 1994). In one embodiment, the human framework has no variation or mutation in its structure or sequence. In a particular embodiment, the framework is a germline framework sequence that has no mutations or variations in its sequence.

As used herein, the term “germline” refers to the nucleotide sequences and amino acid sequences of the antibody genes and gene segments as they are passed from parents to offspring via the germ cells. This germline sequence is distinguished from the nucleotide sequences encoding antibodies in mature B cells which have been altered by recombination and hypermutation events during the course of B cell maturation. An antibody that “utilizes” a particular germline has a nucleotide or amino acid sequence that most closely aligns with that germline nucleotide sequence or with the amino acid sequence that it specifies. Such antibodies frequently are mutated compared with the germline sequence.

In other embodiments, the human framework has minimal variation or mutation from germline sequence in its structure or sequence (e.g., less than 3, 4, 5, 6, 7, 8, 9, or 10 acceptor framework residues have been replaced with donor framework residues to improve binding affinity, see Queen et al., U.S. Pat. No. 5,530,101). In a particular embodiment, a limited number of amino acids in the framework of a humanized immunoglobulin chain (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 amino acids) are chosen to be the same as the amino acids at those positions in the donor sequence (i.e., “back-mutated”), rather than in the acceptor sequence, to increase the affinity of an antibody comprising the humanized immunoglobulin chain for human CD52.

Human framework regions (e.g., of the heavy and/or light chain variable regions) are preferably obtained or derived from a human antibody variable region having sequence similarity to the analogous or equivalent region (e.g., heavy or light chain variable regions) of the antigen-binding region of the donor immunoglobulin (murine anti-CD52 antibody). Other sources of framework regions for portions of human origin of a humanized immunoglobulin include human variable region consensus sequences (See e.g., Kettleborough, C. A. et al., Protein Engineering 4:773-783 (1991); Carter et al., WO 94/04679; Carter U.S. Pat. No. 6,407,213)). For example, the region of the donor sequence of the antibody (e.g., the sequence of the variable region) used to obtain the nonhuman portion can be compared to human sequences as described in Kabat, E. A. et al. Sequences of Proteins of Immunological Interest, Fifth Edition, U.S. Department of Health and Human Services, U.S. Government Printing Office (1991) to select a particular source of the human portions of the humanized immunoglobulin, e.g., a source of the framework regions.

In one embodiment, the framework regions of the humanized immunoglobulin chains are obtained, or derived, from a human Ig variable region having at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90% or at least about 95% overall sequence identity, with the variable region of the nonhuman donor. In a particular embodiment, the framework regions of the humanized immunoglobulin chains are obtained or derived from human variable region framework regions having at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, or at least about 95% overall sequence identity, with the framework regions of the variable region of the nonhuman donor immunoglobulin.

In one embodiment, at least one of the framework regions (FR) of the humanized immunoglobulin is obtained or derived from one or more chains of an antibody of human origin. Thus, the FR can include a FR1 and/or FR2 and/or FR3 and/or FR4 obtained or derived from one or more antibodies of human origin (e.g., from a human immunoglobulin chain, from a human consensus sequence).

The immunoglobulin portions for use in the present invention have sequences identical, or similar, to immunoglobulins from which they are derived or to variants thereof. Such variants include mutants differing by the addition, deletion or substitution (e.g., conservative substitution) of one or more residues, e.g., differeing by up to 3, 4, 5, 6, 7, 8, 9, or 10 residues from the parental sequence by one or more additions, deletions or substitutions. As indicated above, the humanized immunoglobulin of the invention comprises one or more CDRs from one or more of the murine anti-CD52 antibodies (donor antibodies) described herein. Changes in the framework region, such as those which substitute a residue of the framework region of human origin with a residue from the corresponding position of the donor antibody, can be made. One or more mutations, including deletions, insertions and substitutions of one or more amino acids in the framework region, can be made. If desired, framework mutations can be included in a humanized antibody or chain, and sites for mutation can be selected using any suitable method, for example as described in WO 98/06248, the entire teachings of which are incorporated by reference.

It will be appreciated by one of skill in the art that in some cases residues flanking the one or more CDRs of the murine anti-CD52 antibody(ies) may contribute, and in some cases, may be essential, either directly or indirectly, to function (e.g., binding). Thus, in some embodiments, one or more amino acids flanking one or more CDRs (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 flanking amino acids) of the murine framework are also included in the humanized immunoglobulin.

In some embodiments, the human heavy chain framework regions of the humanized antibodies of this invention utilize the human VH3-72 or VH3-23 germline sequence. In some embodiments, the human light chain framework regions of the humanized antibodies of this invention utilize the human Vk2-A18b germline sequence. Back mutations may optionally be made in these FR regions at one or more of the residues as described in the Working Examples below to improve CD52-binding affinity of the humanized antibody.

“Affinity” is a term of art that describes the strength of a binding interaction and typically refers to the overall strength of binding of the immunoglobulin to human CD52.

In a particular embodiment, the immunoglobulin has a binding activity measured as an EC₅₀ value of less than 10 μg/ml (e.g., as determined by flow cytometry). In another embodiment, the immunoglobulin has a binding activity measured as an EC₅₀ value of less than 5.0 μg/ml, or less than 1.0 μg/ml (e.g., as determined by flow cytometry).

In some embodiments, the immunoglobulin binds to human CD52 with an affinity (K_(D); K_(D)=K_(off) (kd)/Kon (ka)) of 300 nM to 1 pM (i.e., 3×10⁻⁷ to 1×10⁻¹²M), preferably 50 nM to 1 pM, more preferably 5 nM to 1 pM and most preferably 1 nM to 1 pM, for example, a K_(D) of 1×10⁻⁷M or less, preferably 1×10⁻⁸M or less, more preferably 1×10⁻⁹ M or less, advantageously 1×10⁻¹⁰ M or less and most preferably 1×10⁻¹¹M or 1 x×10⁻¹² or less; and/or a K_(off) rate constant of 5×10⁻¹ s-1 to 1×10⁻⁷ s-1, preferably 1×10⁻² s-1 to 1×10's-1, more preferably 5×10⁻³ s-1 to 1×10⁻⁵ s-1, for example 5×10⁻¹ s-1 or less, preferably 1×10⁻² s-1 or less, advantageously 1×10⁻³ s-1 or less, more preferably 1×10⁻⁴ s-1 or less, still more preferably 1×10⁻⁵ s-1 or less, and most preferably 1×10's-1 or less as determined by surface plasmon resonance.

As is apparent to one of skill in the art, a variety of methods can be used to confirm that immunoglobulins produced according to methods provided herein and known in the art have the requisite specificity (e.g., binding specificity, epitopic specificity). For example, the binding function of a humanized anti-CD52 immunoglobulin of the invention having binding specificity for human CD52 can be detected using any suitable method, e.g., assays which monitor formation of a complex between humanized immunoglobulin and human CD52 (e.g., a membrane fraction comprising human CD52; a cell bearing human CD52, such as a human T cell, a human B cell; a CHO cell or a recombinant host cell comprising and expressing a nucleic acid encoding human CD52; a peptide (e.g., a synthetic peptide) having an amino acid sequence of CD52; a solid support comprising human CD52).

The ability of an immunoglobulin of the invention (e.g., a humanized immunoglobulin of the invention) to bind to the same epitope on human CD52 as a particular murine, chimeric, or humanized monoclonal antibody, or to bind to an epitope on human CD52 which overlaps with the epitope on human CD52 to which a particular murine, chimeric, or humanized monoclonal antibody binds, can be readily determined using a variety of techniques known to those of skill in the art, including e.g., competitive binding assays. These may involve the use of a labeled form of said particular antibody, and a measurement of the binding of that labeled antibody to human CD52 in the presence and in the absence of an immunoglobulin of the invention.

An “epitope” as used herein includes any protein determinant capable of specific binding to an immunoglobulin. Epitopic determinants generally consist of chemically active surface groupings of molecules such as amino acids or carbohydrate or sugar side chains and generally have specific three dimensional structural characteristics, as well as specific charge characteristics. An epitope may be “linear” or “conformational.” In a linear epitope, all of the points of interaction between the protein and the interacting molecule (such as an antibody) occur linearly along the primary amino acid sequence of the protein. In a conformational epitope, the points of interaction occur across amino acid residues on the protein that are separated from one another. Once a desired epitope on an antigen is determined, it is possible to generate antibodies to that epitope, e.g., using the techniques described in the present invention. Alternatively, during the discovery process, the generation and characterization of antibodies may elucidate information about desirable epitopes. From this information, it is then possible to competitively screen antibodies for binding to the same epitope. An approach to achieve this is to conduct competition studies to find antibodies that competitively bind with one another, i.e., the antibodies compete for binding to the antigen.

In one embodiment, to determine if a test antibody binds to the same or overlapping epitope of a humanized antibody of this invention, one allows the anti-CD52 antibody of the invention to bind to CD52 under saturating conditions and then measures the ability of the test antibody to bind to CD52. If the test antibody is able to bind to CD52 at the same time as the reference anti-CD52 antibody, then the test antibody binds to a different epitope than the reference anti-CD52 antibody. However, if the test antibody is not able to bind to CD52 at the same time, then the test antibody binds to the same epitope, an overlapping epitope, or an epitope that is in close proximity to the epitope bound by the anti-CD52 antibody of the invention. This experiment can be performed using ELISA, RIA, BIACORE™, or flow cytometry. To test whether an anti-CD52 antibody cross-competes with another anti-CD52 antibody, one may use the competition method described above in two directions, i.e., determining if the reference antibody blocks the test antibody and vice versa. In a some embodiment, the experiment is performed using BIACORE™.

Epitope binning can also be useful to characterize the antibodies of this invention. The term “binning” refers to a method to group antibodies based on their antigen binding characteristics. A high throughput process for “binning” antibodies based upon their cross-competition is described in International Patent Application No. WO 03/48731. The “epitope binning” can be investigated by allowing an unlabeled form of an anti-CD52 antibody “A” to bind to a synthetic peptide corresponding to the sequence of CD52 or to CD52 positive cells. Subsequently a labeled second anti-CD52 antibody “B” is added and one can assess the amount of labeled antibody that can bind relative to a control sample where the cells or synthetic peptide have not been exposed previously to anti-CD52 antibody “A.” Alternatively, anti-CD52 antibodies “A” and “B” can both be labeled with different flourochromes or chemicals enabling detection, and one can measure the quantities of both labeled antibodies that can engage the CD52 peptide at the same time using a device capable of detecting the label or measure the amounts of both antibodies that simultaneously engage CD52 positive cells by flow cytometry. Biacore and Octet technologies enable one to investigate the competitive binding of unlabelled forms of antibodies. This use of unlabelled forms of antibodies is desired as the chemical modification of some antibodies can compromise the binding activity. See also the technology described in See also Jia et al., J. Immunol. Methods 288:91-98 (2004), which is useful in performing epitope binning as well.

Also provided herein are portions of the humanized immunoglobulins such as light chains, heavy chains and portions of light and heavy chains. These immunoglobulin portions can be obtained or derived from immunoglobulins (e.g., by reduction and/or cleavage), or produced or expressed by nucleic acids encoding a portion of an immunoglobulin or chain thereof having the desired property (e.g., binds human CD52, sequence similarity). They can be prepared by e.g., de novo synthesis of the relevant portion. Humanized immunoglobulins comprising the desired portions (e.g., antigen-binding region, CDR, FR, C region) of human and nonhuman origin can be produced using synthetic and/or recombinant nucleic acids to prepare constructs (e.g., cDNA) encoding the desired humanized chain. For example, to prepare a portion of an immunoglobulin (e.g., a portion of a chain), one or more stop codons can be introduced at the desired position. Nucleic acid (e.g., DNA) sequences coding for humanized variable regions can be constructed using PCR mutagenesis methods to alter existing DNA sequences (see e.g., Kamman, M., et al., Nucl. Acids Res. 17:5404 (1989)). PCR primers coding for the new CDRs can be hybridized to a DNA template of a previously humanized variable region which is based on the same, or a very similar, human variable region (Sato, K., et al., Cancer Research 53:851-856 (1993)). If a similar DNA sequence is not available for use as a template, a nucleic acid comprising a sequence encoding a variable region sequence can be constructed from synthetic oligonucleotides (see e.g., Kolbinger, F., Protein Engineering 8:971-980 (1993)). A sequence encoding a signal peptide can also be incorporated into the nucleic acid (e.g., on synthesis, upon insertion into a vector). If a signal peptide sequence is unavailable (e.g., not typically present), a signal peptide sequence from another antibody can be used (see, e.g., Kettleborough, C. A., Protein Engineering 4:773-783 (1991)). Using these methods, methods described herein or other suitable methods, variants can readily be produced.

The invention relates to a humanized immunoglobulin that has binding specificity for human CD52 and comprises a humanized light chain and a humanized heavy chain and/or portions thereof. In one embodiment, the humanized immunoglobulin comprises a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 3 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 16; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 4 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 17; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 5 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 18; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 6 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 19; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 7 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 20; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 8 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 21; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 9 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 22; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 10 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 23; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 11 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 24; a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 12 and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 25; or a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 13 and a heavy chain sequence comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 26.

In one embodiment, a humanized immunoglobulin of the invention comprises heavy chain (H)-CDR1, H-CDR2, H-CDR3, light chain (L)-CDR1, L-CDR2, and L-CDR3 whose amino acid sequences are: a) SEQ ID NOs: 51, 59, 69, 29, 36, and 43, respectively; b) SEQ ID NOs: 50, 60, 69, 29, 37, and 43, respectively; c) SEQ ID NOs: 50, 61, 68, 29, 38, and 43, respectively; d) SEQ ID NOs: 50, 61, 69, 29, 36, and 43, respectively; e) SEQ ID NOs: 50, 62, 69, 29, 39, and 43, respectively; 0 SEQ ID NOs: 52, 61, 70, 30, 40, and 43, respectively; g) SEQ ID NOs: 53, 63, 71, 31, 36, and 44, respectively; h) SEQ ID NOs: 54, 64, 71, 31, 36, and 45, respectively; i) SEQ ID NOs: 55, 63, 72, 31, 36, and 46, respectively; j) SEQ ID NOs: 56, 65, 73, 32, 41, and 47, respectively; k) SEQ ID NOs: 56, 65, 294, 32, 41, and 47; or 1) SEQ ID NOs: 56, 66, 74, 33, 41, and 48, respectively.

In another embodiment, a humanized immunoglobulin of this invention comprises H-CDR3 and L-CDR3 whose sequences are a) SEQ ID NOs: 69 and 43, respectively; b) SEQ ID NOs: 68 and 43, respectively; c) SEQ ID NOs: 70 and 43, respectively; d) SEQ ID NOs: 71 and 44, respectively; e) SEQ ID NOs: 71 and 45, respectively; 0 SEQ ID NOs: 72 and 46, respectively; g) SEQ ID NOs: 73 and 47, respectively; h) SEQ ID NOs: 294 and 47, respectively; or i) SEQ ID NOs: 74 and 48, respectively.

In another embodiment, the humanized immunoglobulin has binding specificity for human CD52 and comprises a light chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 29, SEQ ID NO: 30, SEQ ID NO: 31, SEQ ID NO: 32, SEQ ID NO: 33, SEQ ID NO: 34, SEQ ID NO: 35, SEQ ID NO: 36, SEQ ID NO: 37, SEQ ID NO: 38, SEQ ID NO: 39, SEQ ID NO: 40, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43, SEQ ID NO: 44, SEQ ID NO: 45, SEQ ID NO: 46, SEQ ID NO: 47, and SEQ ID NO: 48, or a combination thereof; and a heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 49, SEQ ID NO: 50, SEQ ID NO: 51, SEQ ID NO: 52, SEQ ID NO: 53, SEQ ID NO: 54, SEQ ID NO: 55, SEQ ID NO: 56, SEQ ID NO: 57, SEQ ID NO: 58, SEQ ID NO: 59, SEQ ID NO: 60, SEQ ID NO: 61, SEQ ID NO: 62, SEQ ID NO: 63, SEQ ID NO: 64, SEQ ID NO: 65, SEQ ID NO: 66, SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO: 69, SEQ ID NO: 70, SEQ ID NO: 71, SEQ ID NO: 72, SEQ ID NO: 73, SEQ ID NO: 74, and SEQ ID NO: 294, or a combination thereof, wherein the humanized immunoglobulin is not Campath®.

In another embodiment, the humanized immunoglobulin that has a binding specificity for human CD52 comprises a light chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12 or SEQ ID NO: 13, and a heavy chain comprising one or more CDRs (e.g., all three CDRs) of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23, SEQ ID NO: 24, SEQ ID NO: 25, SEQ ID NO: 26, or SEQ ID NO: 137, wherein the humanized immunoglobulin is not Campath®.

The invention also relates to a humanized immunoglobulin light chain of the humanized immunoglobulin described herein. In one embodiment, the humanized immunoglobulin light chain comprises one or more CDRs selected from the group consisting of SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 29, SEQ ID NO: 30, SEQ ID NO: 31, SEQ ID NO: 32, SEQ ID NO: 33, SEQ ID NO: 34, SEQ ID NO: 35, SEQ ID NO: 36, SEQ ID NO: 37, SEQ ID NO: 38, SEQ ID NO: 39, SEQ ID NO: 40, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43, SEQ ID NO: 44, SEQ ID NO: 45, SEQ ID NO: 46, SEQ ID NO: 47, and SEQ ID NO: 48, and a combination thereof, wherein the humanized immunoglobulin light chain is not the light chain of Campath®. For example, the humanized antibody has L-CDR1, L-CDR2, and L-CDR3 whose amino acid sequences are: a) SEQ ID NOs: 29, 36, and 43, respectively; b) SEQ ID NOs: 29, 37, and 43, respectively; c) SEQ ID NOs: 29, 38, and 43, respectively; d) SEQ ID NOs: 29, 36, and 43, respectively; e) SEQ ID NOs: 29, 39, and 43, respectively; 0 SEQ ID NOs: 30, 40, and 43, respectively; g) SEQ ID NOs: 31, 36, and 44, respectively; h) SEQ ID NOs: 31, 36, and 45, respectively; i) SEQ ID NOs: 31, 36, and 46, respectively; j) SEQ ID NOs: 32, 41, and 47, respectively; or k) SEQ ID NOs: 33, 41, and 48, respectively.

The invention also relates to humanized heavy chain comprising one or more CDRs selected from the group consisting of SEQ ID NO: 49, SEQ ID NO: 50, SEQ ID NO: 51, SEQ ID NO: 52, SEQ ID NO: 53, SEQ ID NO: 54, SEQ ID NO: 55, SEQ ID NO: 56, SEQ ID NO: 57, SEQ ID NO: 58, SEQ ID NO: 59, SEQ ID NO: 60, SEQ ID NO: 61, SEQ ID NO: 62, SEQ ID NO: 63, SEQ ID NO: 64, SEQ ID NO: 65, SEQ ID NO: 66, SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO: 69, SEQ ID NO: 70, SEQ ID NO: 71, SEQ ID NO: 72, SEQ ID NO: 73, SEQ ID NO: 74, and SEQ ID NO: 294, or a combination thereof, wherein the humanized immunoglobulin heavy chain is not the heavy chain of Campath®. For example, the humanized antibody has H-CDR1, H-CDR2, and H-CDR3 whose amino acid sequences are: a) SEQ ID NOs: 51, 59, and 69, respectively; b) SEQ ID NOs: 50, 60, and 69, respectively; c) SEQ ID NOs: 50, 61, and 68, respectively; d) SEQ ID NOs: 50, 61, and 69, respectively; e) SEQ ID NOs: 50, 62, and 69, respectively; 0 SEQ ID NOs: 52, 61, and 70, respectively; g) SEQ ID NOs: 53, 63, and 71, respectively; h) SEQ ID NOs: 54, 64, and 71, respectively; i) SEQ ID NOs: 55, 63, and 72, respectively; j) SEQ ID NOs: 56, 65, and 73, respectively; k) SEQ ID NOs: 56, 65, and 294; or 1) SEQ ID NOs: 56, 66, and 74, respectively.

In one embodiment, a humanized antibody of this invention comprises a light chain comprising a variable domain (V_(L)) sequence of one of SEQ ID NOs: 102, 138, 145-148, 153-157, and 164-168. In a related embodiment, the humanized antibody comprises a light chain whose amino acid sequence comprises or consists of one of SEQ ID NOs: 273, 275, 278, 280, and 282.

In one embodiment, a humanized antibody of this invention comprises a heavy chain comprising a variable domain (V_(H)) sequence of one of SEQ ID NOs: 103, 136, 137, 139-144, 149-152, and 158-163. In a related embodiment, the humanized antibody comprises a heavy chain whose amino acid sequence comprises or consists of one of SEQ ID NOs: 272, 274, 276, 277, 279, and 281.

In some embodiments, a humanized antibody of this invention comprises a V_(H) and a V_(L) whose amino acid sequences comprise or consist of

a) SEQ ID NOs: 103 and 102, respectively (4B10-H1/K1);

b) SEQ ID NOs: 136 and 138, respectively (7F11-SFD1/K2);

c) SEQ ID NOs: 137 and 138, respectively (7F11-SFD2/K2)

d) SEQ ID NO: 139 and one of SEQ ID NOs: 145-148, respectively (e.g., SEQ ID NOs: 139 and 146, respectively (2C3-SFD1/K11); and SEQ ID NOs: 139 and 147, respectively (2C3-SFD1/K12));

e) SEQ ID NO: 140 and one of SEQ ID NOs: 145-148, respectively;

f) SEQ ID NO: 141 and one of SEQ ID NOs: 145-148, respectively;

g) SEQ ID NO: 142 and one of SEQ ID NOs: 145-148, respectively;

h) SEQ ID NO: 143 and one of SEQ ID NOs: 145-148, respectively;

i) SEQ ID NO: 144 and one of SEQ ID NOs: 145-148, respectively;

j) SEQ ID NO: 149 and one of SEQ ID NOs: 153-157, respectively (e.g., SEQ ID NOs: 149 and 155, respectively (12G6-SFD1/K11); SEQ ID NOs: 149 and 156, respectively (12G6-SFD1/K12); and SEQ ID NOs: 149 and 157, respectively (12G6-SFD1/K13));

k) SEQ ID NO: 150 and one of SEQ ID NOs: 153-157, respectively;

l) SEQ ID NO: 151 and one of SEQ ID NOs: 153-157, respectively;

m) SEQ ID NO: 152 and one of SEQ ID NOs: 153-157, respectively;

n) SEQ ID NO: 158 and one of SEQ ID NOs: 164-168, respectively (e.g., SEQ ID NOs: 158 and 165, respectively (9D9-H10/K12); and SEQ ID NOs: 158 and 166, respectively (9D9-H10/K13));

o) SEQ ID NO: 159 and one of SEQ ID NOs: 164-168, respectively (e.g., SEQ ID NOs: 159 and 165, respectively (9D9-H11/K12); and SEQ ID NOs: 159 and 166, respectively (9D9-H11/K13));

p) SEQ ID NO: 160 and one of SEQ ID NOs: 164-168, respectively;

q) SEQ ID NO: 161 and one of SEQ ID NOs: 164-168, respectively (e.g., SEQ ID NOs: 161 and 166, respectively (9D9-H16/K13));

r) SEQ ID NO: 162 and one of SEQ ID NOs: 164-168, respectively; or

s) SEQ ID NO: 163 and one of SEQ ID NOs: 164-168, respectively (e.g., SEQ ID NOs: 163 and 166, respectively (9D9-H18/K13)).

The antibodies included in the parentheses are further described below in the working examples.

In one embodiment, a humanized antibody of this invention comprises a light chain (LC) and a heavy chain (HC) whose amino acid sequences comprise or consist of a) SEQ ID NOs: 273 and 272, respectively; b) SEQ ID NOs: 275 and 274, respectively; c) SEQ ID NOs: 278 and 276, respectively; d) SEQ ID NOs: 278 and 277, respectively; e) SEQ ID NOs: 280 and 279, respectively; or f) SEQ ID NOs: 282 and 281, respectively.

This invention also provides anti-human CD52 antibodies (except those, in any, known in the prior art) that binds to the same epitope as, or competes or cross-competes with, an antibody exemplified herein. These antibodies can be, for example, humanized, chimeric, or mouse antibodies. For example, the invention provides anti-human CD52 antibodies that bind to the same epitope as, or competes or cross-competes with, one of mouse antibodies 8G3, 4F7, 9D9, 11C11, 3G7, 5F7, 12G6, 23E6, 2C3, 7F11, and 4B10, and humanized and chimeric versions of these mouse antibodies. The ability of an antibody to bind to the same epitope as, or competes or cross-competes with a reference antibody can be determined as described above. For example, we have found that the CD52 epitope bound by the humanized antibodies 2C3-SFD1/K12 and 12G6-SFD1/K12 includes residues 7, 8, and 11 in SEQ ID NO: 104, and that the epitope bound by the humanized antibody 9D9-H16/K13 includes residues 4 and 11 in SEQ ID NO: 104. Thus, in some embodiments, this invention provides anti-CD52 antibodies that bind to the same epitope as, or competes or cross-competes with, those humanized antibodies.

If desired, for example, for diagnostic or assay purposes (e.g., imaging to allow, for example, monitoring of therapies), the humanized immunoglobulin (e.g., antigen-binding fragment thereof) can comprise a detectable label. Suitable detectable labels and methods for labeling a humanized immunoglobulin or antigen-binding fragment thereof are well known in the art. Suitable detectable labels include, for example, a radioisotope (e.g., as Indium-111, Technnetium-99m or Iodine-131), positron emitting labels (e.g., Fluorine-19), paramagnetic ions (e.g., Gadlinium (III), Manganese (II)), an epitope label (tag), an affinity label (e.g., biotin, avidin), a spin label, an enzyme, a fluorescent group or a chemiluminescent group. When labels are not employed, complex formation (e.g., between humanized immunoglobulin and human CD52) can be determined by surface plasmon resonance, ELISA, FACS, or other suitable methods.

Anti-CD52 antibodies used in the invention also may be conjugated, via, for example, chemical reactions or genetic modifications, to other moieties (e.g., pegylation moieties) that improve the antibodies' pharmacokinetics such as half-life. In some embodiments, the anti-CD52 antibodies used in this invention can be linked to a suitable cytokine via, e.g., chemical conjugation or genetic modifications (e.g., appending the coding sequence of the cytokine in frame to an antibody coding sequence, thereby creating an antibody: cytokine fusion protein).

The invention also relates to immunoconjugates in which the humanized immunoglobulin (e.g., antigen-binding fragment thereof) of the invention is coupled to another therapeutic agent, such as a bioactive compound (e.g., cytokines, superantigens, cytotoxic agents and toxins). For example, the humanized immunoglobulin that has binding specificity for human CD52 (e.g., antigen binding fragment thereof) can be coupled to a biological protein, a molecule of plant or bacterial origin (or derivative thereof), an interleukin-2 antibody or diptheria toxin antibodies.

Mouse Monoclonal Immunoglobulins

As described herein, mouse monoclonal immunoglobulins having binding specificity for human CD52 have been produced. Humanized and chimeric antibodies of this invention can be derived from the mouse monoclonal antibodies of this invention. That is, in some embodiments, humanized and chimeric anti-CD52 antibodies of the invention comprise sequences taken from a mouse monoclonal antibody of the invention, such as one or more CDR sequences. A mouse monoclonal immunoglobulin of this invention comprises a light chain and a heavy chain that have CDR amino acid sequences which differ from the CDR amino acid sequences of known mouse anti-CD52 monoclonal antibodies (e.g., from CF1D12).

As used herein, the term “mouse monoclonal immunoglobulin” refers to an immunoglobulin containing light chain CDRs (L-CDR1, L-CDR2 and L-CDR3) and heavy chain CDRs (H-CDR1, H-CDR2 and H-CDR3) of a murine anti-human CD52 antibody, and framework and constant regions of murine origin. Mouse monoclonal immunoglobulins are homogeneous antibodies of a single specificity prepared, for example, by the use of hybridoma technology or recombinant methods.

The invention relates to the mouse monoclonal immunoglobulins described herein, including antigen-binding fragments (i.e., portions) of the mouse monoclonal immunoglobulins, the light chains of the mouse monoclonal immunoglobulins, the heavy chains of the mouse monoclonal immunoglobulins, and fragments of these heavy and light chains. In a particular embodiment, the mouse monoclonal antibody is the mouse 8G3.25.3.5 (also called GENZ 8G3.25.3.5 or 8G3), mouse GMA 4G7.F3 (also called 4G7.F3 or 4G7), mouse GMA 9D9. A2 (also called 9D9. A2 or 9D9), mouse GMA 11C11.C5 (also called 11C11.C5 or 11C11), mouse GMA 3G7.E9 (also called 3G7.E9 or 3G7), mouse 5F7.1.1.4 (also called GENZ 5F7.1.1.4 or 5F7), mouse 12G6.15.1.2 (also called GENZ 12G6.15.1.2 or 2G6), mouse 23E6.2.2.1 (also called GENZ 23E6.2.2.1 or 23E6), mouse 2C3.3.8.1 (also called GENZ 2C3.3.8.1 or 2C3), mouse 7F11.1.9.7 (also called GENZ 7F11.1.9.7 or 7F11), or mouse 4B10.1.2.4 (also called GENZ 4B10.1.2.4 or 4B10). The invention relates to mature mouse monoclonal immunoglobulin, such as the mouse monoclonal immunoglobulin following processing to remove the heavy and light chain signal peptides and/or to the glycosylated immunoglobulin. The invention also relates to immature or precursor protein, such as a mouse immunoglobulin light chain or a mouse immunoglobulin heavy chain comprising a signal peptide. The invention also relates to nucleic acid molecules (e.g., vectors) that encode these immature or mature proteins, to host cells that comprise such nucleic acids and to methods of producing these immature and mature proteins.

The binding function of a mouse monoclonal immunoglobulin having binding specificity for human CD52 can be detected using any suitable method, for example using assays which monitor formation of a complex between mouse monoclonal immunoglobulin and human CD52 (e.g., a membrane fraction comprising human CD52, or a cell bearing human CD52, such as a human T cell, a human B cell, CHO cell or a recombinant host cell comprising a nucleic acid encoding human CD52; a peptide (e.g., a synthetic peptide) having an amino acid sequence of CD52).

Also provided herein are portions of the murine immunoglobulins which include light chains, heavy chains and portions of light and heavy chains. These immunoglobulin portions can be obtained or derived from immunoglobulins (e.g., by reduction and/or cleavage), or nucleic acids encoding a portion of an immunoglobulin or chain thereof having the desired property (e.g., binds human CD52, sequence similarity) can be produced and expressed. They can be prepared by e.g., de novo synthesis of a portion of mouse monoclonal immunoglobulins comprising the desired portions (e.g., antigen-binding region, CDR, FR, and/or C region) of murine origin can be produced using synthetic and/or recombinant nucleic acids to prepare constructs (e.g., cDNA) encoding the desired monoclonal immunoglobulin chain. To prepare a portion of a chain, one or more stop codons can be introduced at the desired position. A sequence encoding a signal peptide can also be incorporated into the nucleic acid (e.g., on synthesis, upon insertion into a vector). If the natural signal peptide sequence is unavailable, a signal peptide sequence from another antibody can be used (see, e.g., Kettleborough, C. A., Protein Engineering 4:773-783 (1991)). Using these methods, methods described herein or other suitable methods, variants can be readily produced.

In one embodiment, a mouse monoclonal immunoglobulin of this invention comprises a light chain comprising SEQ ID NO: 3 and a heavy chain comprising SEQ ID NO: 16; a light chain comprising SEQ ID NO: 4 and a heavy chain comprising SEQ ID NO: 17; a light chain comprising SEQ ID NO: 5 and a heavy chain comprising SEQ ID NO: 18; a light chain comprising SEQ ID NO: 6 and a heavy chain comprising SEQ ID NO: 19; a light chain comprising SEQ ID NO: 7 and a heavy chain comprising SEQ ID NO: 20; a light chain comprising SEQ ID NO: 8 and a heavy chain comprising SEQ ID NO: 21; a light chain comprising SEQ ID NO: 9 and a heavy chain comprising SEQ ID NO: 22; a light chain comprising SEQ ID NO: 10 and a heavy chain comprising SEQ ID NO: 23; a light chain comprising SEQ ID NO: 11 and a heavy chain comprising SEQ ID NO: 24; a light chain comprising SEQ ID NO: 12 and a heavy chain comprising SEQ ID NO: 25; or a light chain comprising SEQ ID NO: 13 and a heavy chain comprising SEQ ID NO: 26.

In another embodiment, the invention also relates to a mouse monoclonal antibody that has binding specificity for human CD52, comprising a light chain variable region selected from the group consisting of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9; SEQ ID NO: 10; SEQ ID NO: 11, SEQ ID NO: 12, and SEQ ID NO: 13; and a heavy chain variable region selected from the group consisting of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23; SEQ ID NO: 24, SEQ ID NO: 25 and SEQ ID NO: 26.

If desired, for example, for diagnostic or assay purposes (e.g., imaging), the mouse monoclonal immunoglobulin (e.g., antigen binding fragment thereof) can comprise a detectable label. Suitable detectable labels and methods for labeling a mouse monoclonal immunoglobulin are well known in the art. Suitable detectable labels include, for example, a radioisotope (e.g., as Indium-111, Technnetium-99m or Iodine-131), positron emitting labels (e.g., Fluorine-19), paramagnetic ions (e.g., Gadlinium (III), Manganese (II)), an epitope label (tag), an affinity label (e.g., biotin, avidin), a spin label, an enzyme, a fluorescent group or a chemiluminescent group. When labels are not employed, complex formation (e.g., between mouse monoclonal immunoglobulin and CD52) can be determined by surface plasmon resonance or other suitable methods. All suitable methods and techniques described above for humanized antibodies of this invention can also be used herein.

Chimeric Immunoglobulins

As described herein, chimeric immunoglobulins having binding specificity for human CD52 have been produced. The chimeric immunoglobulin comprises a chimeric light chain and/or a chimeric heavy chain that have amino acid sequences which differ from the amino acid sequence of known chimeric antibodies having binding specificity for human CD52.

As used herein, the term “chimeric immunoglobulin” refers to a recombinant protein that contains the variable domains including the complementarity determining regions (CDRs) of an antibody derived from one species, preferably a murine anti-human CD52 monoclonal antibody, while the constant domains of the antibody molecule are derived from those of a different species, e.g., from a human antibody.

The invention relates to the chimeric immunoglobulins described herein, including antigen-binding fragments (i.e., portions) of the chimeric immunoglobulins, the chimeric light chains and chimeric heavy chains of the chimeric immunoglobulins and fragments of these chimeric light and heavy chains. The invention relates to mature chimeric immunoglobulin, such as the chimeric immunoglobulin following processing to remove the heavy and light signal peptides and/or to the glycosylated immunoglobulin. The invention also relates to immature or precursor protein, such as a chimeric heavy chain comprising a signal peptide. The invention also relates to nucleic acid molecules (e.g., vectors) that encode these immature or mature proteins, to host cells that comprise such nucleic acids and to methods of producing these immature and mature proteins.

The binding function of a chimeric immunoglobulin having binding specificity for human CD52 can be detected using any suitable method, for example using assays which monitor formation of a complex between chimeric immunoglobulin and human CD52 (e.g., a membrane fraction comprising human CD52, on a cell bearing human CD52, such as a human T cell, a human B cell, CHO cell or a recombinant host cell comprising a nucleic acid encoding human CD52, a peptide (e.g., synthetic peptide) having an amino acid sequence of CD52).

Also provided herein are portions of the chimeric immunoglobulins which include light chains, heavy chains and portions of light and heavy chains. These immunoglobulin portions can be obtained or derived from immunoglobulins (e.g., by reduction and/or cleavage), or nucleic acids encoding a portion of an immunoglobulin or chain thereof having the desired property (e.g., binds human CD52, sequence similarity) can be produced and expressed. They may be prepared by e.g., de novo synthesis of a portion. Chimeric immunoglobulins comprising the desired portions (e.g., antigen-binding region, CDR, FR, and/or C region) of human and non-human origin can be produced using synthetic and/or recombinant nucleic acids to prepare constructs (e.g., cDNA) encoding the desired chimeric chain. To prepare a portion of a chain, one or more stop codons can be introduced at the desired position. A sequence encoding a signal peptide can also be incorporated into the nucleic acid (e.g., on synthesis, upon insertion into a vector). If the natural signal peptide sequence is unavailable (e.g., typically not present), a signal peptide sequence from another antibody can be used (see, e.g., Kettleborough, C. A., Protein Engineering 4:773-783 (1991)). Using these methods, methods described herein or other suitable methods, variants can be readily produced.

In one embodiment, a chimeric immunoglobulin of this invention comprises the light chain variable region of SEQ ID NO: 3 and the heavy chain variable region of SEQ ID NO: 16; the light chain variable region of SEQ ID NO: 4 and the heavy chain variable region of SEQ ID NO: 17; the light chain variable region of SEQ ID NO: 5 and the heavy chain variable region of SEQ ID NO: 18; the light chain variable region of SEQ ID NO: 6 and the heavy chain variable region of SEQ ID NO: 19; the light chain variable region of SEQ ID NO: 7 and the heavy chain variable region of SEQ ID NO: 20; the light chain variable region of SEQ ID NO: 8 and the heavy chain variable region of SEQ ID NO: 21; the light chain variable region of SEQ ID NO: 9 and the heavy chain variable region of SEQ ID NO: 22; the light chain variable region of SEQ ID NO: 10 and the heavy chain variable region of SEQ ID NO: 23; the light chain variable region of SEQ ID NO: 11 and the heavy chain variable region of SEQ ID NO: 24; the light chain variable region of SEQ ID NO: 12 and the heavy chain variable region of SEQ ID NO: 25; or the light chain variable region of SEQ ID NO: 13 and the heavy chain variable region of SEQ ID NO: 26.

The invention also relates to a chimeric antibody that has binding specificity for human CD52, comprising a light chain variable region sequence selected from the group consisting of: the light chain variable region of SEQ ID NO: 3, the light chain variable region of SEQ ID NO: 4, the light chain variable region of SEQ ID NO: 5, the light chain variable region of SEQ ID NO: 6, the light chain variable region of SEQ ID NO: 7, the light chain variable region of SEQ ID NO: 8, the light chain variable region of SEQ ID NO: 9, the light chain variable region of SEQ ID NO: 10, the light chain variable region of SEQ ID NO: 11, the light chain variable region of SEQ ID NO: 12 and the light chain variable region of SEQ ID NO: 13, and a heavy chain variable region sequence selected from the group consisting of: the heavy chain variable region of SEQ ID NO: 16, the heavy chain variable region of SEQ ID NO: 17, the heavy chain variable region of SEQ ID NO: 18, the heavy chain variable region of SEQ ID NO: 19, the heavy chain variable region of SEQ ID NO: 20, the heavy chain variable region of SEQ ID NO: 21, the heavy chain variable region of SEQ ID NO: 22, the heavy chain variable region of SEQ ID NO: 23, the heavy chain variable region of SEQ ID NO: 24, the heavy chain variable region of SEQ ID NO: 25 and the heavy chain variable region of SEQ ID NO: 26.

The invention also relates to a chimeric light chain comprising the variable region of SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, or SEQ ID NO: 13.

The invention also relates to a chimeric heavy chain comprising the variable region of SEQ ID NO: 16, SEQ ID NO: 17, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 23; SEQ ID NO: 24, SEQ ID NO: 25 or SEQ ID NO: 26

If desired, for example, for diagnostic or assay purposes (e.g., imaging), the chimeric immunoglobulin (e.g., antigen-binding fragment thereof) can comprise a detectable label. Suitable detectable labels and methods for labeling a chimeric immunoglobulin are well known in the art. Suitable detectable labels include, for example, a radioisotope (e.g., as Indium-111, Technnetium-99m or Iodine-131), positron emitting labels (e.g., Fluorine-19), paramagnetic ions (e.g., Gadlinium (III), Manganese (II)), an epitope label (tag), an affinity label (e.g., biotin, avidin), a spin label, an enzyme, a fluorescent group or a chemiluminescent group. When labels are not employed, complex formation (e.g., between chimeric immunoglobulin and human CD52) can be determined by surface plasmon resonance or other suitable methods. All suitable methods and techniques described above for humanized antibodies of this invention can also be used herein.

Nucleic Acids and Recombinant Vectors

The present invention also relates to isolated and/or recombinant (including, e.g., essentially pure) nucleic acids comprising sequences which encode a humanized immunoglobulin, humanized light chain, humanized heavy chain, mouse monoclonal immunoglobulin, mouse immunoglobulin light chain, mouse immunoglobulin heavy chain, chimeric immunoglobulin, chimeric light chain or chimeric heavy chain of the present invention.

Nucleic acids referred to herein as “isolated” or “purified” are nucleic acids which have been separated away from the nucleic acids of the genomic DNA or cellular RNA of their source of origin (e.g., as they exist in cells or in a mixture of nucleic acids such as a library), and include nucleic acids obtained by methods described herein or other suitable methods, including essentially pure nucleic acids, nucleic acids produced by chemical synthesis, by combinations of biological and chemical methods, and recombinant nucleic acids which are isolated (see e.g., Daugherty, B. L. et al., Nucleic Acids Res., 19(9): 2471-2476 (1991); Lewis, A. P. and J. S. Crowe, Gene, 101: 297-302 (1991)).

Nucleic acids referred to herein as “recombinant” are nucleic acids which have been produced by recombinant DNA methodology, including those nucleic acids that are generated by procedures which rely upon a method of artificial recombination, such as the polymerase chain reaction (PCR) and/or cloning into a vector using restriction enzymes. “Recombinant” nucleic acids are also those that result from recombination events that occur through the natural mechanisms of cells, but are selected for after the introduction to the cells of nucleic acids designed to allow and make probable a desired recombination event.

The present invention also relates more specifically to isolated and/or recombinant nucleic acids comprising a nucleotide sequence which encodes a humanized immunoglobulin, mouse immunoglobulin or chimeric immunoglobulin that has binding specificity for human CD52 (e.g., a humanized immunoglobulin of the present invention in which the nonhuman portion (e.g., the CDRs) is derived from a murine anti-CD52 monoclonal antibody; a mouse immunoglobulin of the present invention; or a chimeric immunoglobulin of the present invention in which the nonhuman portion (e.g., the V_(H) and V_(L)) is derived from a murine anti-CD52 monoclonal antibody) or portion (e.g., antigen-binding portion) thereof (e.g., heavy or light chain thereof).

Nucleic acids of the present invention can be used to produce humanized immunoglobulins having binding specificity for human CD52, mouse immunoglobulins having binding specificity for human CD52 and chimeric immunoglobulins having binding specificity for human CD52. For example, a nucleic acid (e.g., DNA (such as cDNA), or RNA) or one or more nucleic acids encoding a humanized immunoglobulin, mouse immunoglobulin or chimeric immunoglobulin of the present invention can be incorporated into a suitable construct (e.g., a recombinant vector) for further manipulation of sequences or for production of the encoded immunoglobulins in suitable host cells.

Constructs or vectors (e.g., expression vectors) suitable for the expression of a humanized immunoglobulin having binding specificity for human CD52, mouse immunoglobulin having binding specificity for human CD52 or chimeric immunoglobulin having binding specificity for human CD52 are also provided. A variety of vectors are available, including vectors which are maintained in single copy or multiple copies in a host cell, or which become integrated into the host cell's chromosome(s). The constructs or vectors can be introduced into a suitable host cell, and cells which express a humanized immunoglobulin, mouse immunoglobulin or chimeric immunoglobulin of the present invention, can be produced and maintained in culture. A single vector or multiple vectors can be used for the expression of a humanized immunoglobulin, mouse immunoglobulin or chimeric immunoglobulin having binding specificity for human CD52.

Suitable expression vectors, for example mammalian cell expression vectors, can also contain a number of components, including, but not limited to one or more of the following: an origin of replication; a selectable marker gene; one or more expression control elements, such as a transcriptional control element (e.g., a promoter, an enhancer, a terminator), and/or one or more translation signals; a signal sequence or leader sequence for membrane targeting or secretion. In a construct or vector, a signal peptide sequence can be provided by the construct or vector or other source. For example, the transcriptional and/or translational signals of an immunoglobulin can be used to direct expression.

A promoter can be provided for expression in a suitable host cell. Promoters can be constitutive or inducible. For example, a promoter can be operably linked to a nucleic acid encoding a humanized immunoglobulin or immunoglobulin chain, such that it directs expression of the encoded polypeptide. A variety of suitable promoters for prokaryotic (e.g., lac, tac, T3, T7 promoters for E. coli) and eukaryotic (e.g., yeast alcohol dehydrogenase (ADH1), SV40, CMV) hosts are available. Those of skill in the art will be able to select the appropriate promoter for expressing an anti-CD52 antibody or portion thereof of the invention.

In addition, the vectors (e.g., expression vectors) typically comprise a selectable marker for selection of host cells carrying the vector, and, in the case of a replicable vector, an origin of replication. Genes encoding products which confer antibiotic or drug resistance are common selectable markers and may be used in prokaryotic (e.g., β-lactamase gene (ampicillin resistance), Tet gene (tetracycline resistance) and eukaryotic cells (e.g., neomycin (G418 or geneticin), gpt (mycophenolic acid), ampicillin, or hygromycin resistance genes). Dihydrofolate reductase marker genes permit selection with methotrexate in a variety of hosts. Genes encoding the gene product of auxotrophic markers of the host (e.g., LEU2, URA3, HIS3) are often used as selectable markers in yeast. Use of viral (e.g., baculovirus) or phage vectors, and vectors which are capable of integrating into the genome of the host cell, such as retroviral vectors, are also contemplated.

The invention thus relates to isolated nucleic acid molecules that encode the humanized immunoglobulin, humanized light chain, humanized heavy chain, mouse immunoglobulin, mouse immunoglobuin light chain, mouse immunoglobuin heavy chain, chimeric immunoglobulin, chimeric light chain, or chimeric heavy chain of this invention. The invention also relates to isolated nucleic acid molecules that encode an antigen-binding portion of the immunoglobulins and their chains. Polypeptide sequences encoded by the nucleic acids of this invention are described above and in the following Examples.

In some embodiments, a nucleic acid and vector of this invention encodes a heavy chain (or an antigen-binding portion thereof) or a light chain (or an antigen-binding portion thereof) of this invention. A host cell containing both the heavy chain-encoding nucleic acid and the light chain-encoding nucleic acid can be used to make an antibody comprising the heavy and light chain (or an antigen-binding portion of the antibody). The heavy chain-encoding nucleic acid and the light chain-encoding nucleic acid can be placed on separate expression vectors. They can also be placed on a single expression vector under the same or different expression control. See, e.g., Cabilly U.S. Pat. No. 6,331,415; Fang U.S. Pat. No. 7,662,623.

Method of Producing Immunoglobulins Having Specificity for Human CD52

Another aspect of the invention relates to a method of making an anti-human CD52 antibody of this invention. The antibody of this invention can be produced, for example, by the expression of one or more recombinant nucleic acids encoding the antibody in a suitable host cell. The host cell can be produced using any suitable method. For example, the expression constructs (e.g., the one or more vectors, e.g., a mammalian cell expression vector) described herein can be introduced into a suitable host cell, and the resulting cell can be maintained (e.g., in culture, in an animal, in a plant) under conditions suitable for expression of the construct(s) or vector(s). Suitable host cells can be prokaryotic, including bacterial cells such as E. coli (e.g., strain DHSα™ (Invitrogen, Carlsbad, Calif.)), B. subtilis and/or other suitable bacteria; eukaryotic cells, such as fungal or yeast cells (e.g., Pichia pastoris, Aspergillus sp., Saccharomyces cerevisiae, Schizosaccharomyces pombe, Neurospora crassa), or other lower eukaryotic cells, and cells of higher eukaryotes such as those from insects (e.g., Drosophila Schnieder S2 cells, Sf9 insect cells (WO 94/26087 (O'Connor), TN5B1-4 (HIGH 5) insect cells (Invitrogen), mammals (e.g., COS cells, such as COS-1 (ATCC Accession No. CRL-1650) and COS-7 (ATCC Accession No. CRL-1651), CHO (e.g., ATCC Accession No. CRL-9096), CHO DG44 (Urlaub, G. and Chasin, L A., Proc. Natl. Acac. Sci. USA, 77(7):4216-4220 (1980)), 293 (ATCC Accession No. CRL-1573), HeLa (ATCC Accession No. CCL-2), CV1 (ATCC Accession No. CCL-70), WOP (Dailey, L., et al., J. Virol., 54:739-749 (1985)), 3T3, 293T (Pear, W. S., et al., Proc. Natl. Acad. Sci. U.S.A., 90:8392-8396 (1993)), NS0 cells, SP2/0 cells, HuT 78 cells and the like)), or plants (e.g., tobacco, lemna (duckweed), and algae). (See, for example, Ausubel, F. M. et al., eds. Current Protocols in Molecular Biology, Greene Publishing Associates and John Wiley & Sons Inc. (1993)). In some embodiments, the host cell is not part of a multicellular organism (e.g., plant or animal), e.g., it is an isolated host cell or is part of a cell culture.

The present invention also relates to cells comprising a nucleic acid, e.g., a vector, of the invention (e.g., an expression vector). For example, a nucleic acid (i.e., one or more nucleic acids) encoding the heavy and light chains of a humanized immunoglobulin, the heavy and light chains of mouse immunoglobulin, or the heavy and light chains of a chimeric immunoglobulin, said immunoglobulin having binding specificity for human CD52, or a construct (i.e., one or more constructs, e.g., one or more vectors) comprising such nucleic acid(s), can be introduced into a suitable host cell by a method appropriate to the host cell selected (e.g., transformation, transfection, electroporation, infection), with the nucleic acid(s) being, or becoming, operably linked to one or more expression control elements (e.g., in a vector, in a construct created by processes in the cell, integrated into the host cell genome). Host cells can be maintained under conditions suitable for expression (e.g., in the presence of inducer, suitable media supplemented with appropriate salts, growth factors, antibiotic, nutritional supplements, etc.), whereby the encoded polypeptide(s) are produced. If desired, the encoded protein (e.g., humanized immunoglobulin, mouse immunoglobulin, chimeric immunoglobulin) can be isolated, for example, from the host cells, culture medium, or milk. This process encompasses expression in a host cell (e.g., a mammary gland cell) of a transgenic animal or plant (e.g., tobacco) (see e.g., WO 92/03918).

Fusion proteins can be produced in which an immunoglobulin portion (e.g., a humanized immunoglobulin; immunoglobulin chain) is linked to a non-immunoglobulin moiety (i.e., a moiety which does not occur in immunoglobulins as found in nature) in an N-terminal location, C-terminal location or internal to the fusion protein. For example, some embodiments can be produced by the insertion of a nucleic acid encoding an immunoglobulin sequence(s) into a suitable expression vector, such as a pET vector (e.g., pET-15b, Novagen), a phage vector (e.g., pCANTAB 5 E, Pharmacia), or other vector (e.g., pRIT2T Protein A fusion vector, Pharmacia). The resulting construct can be introduced into a suitable host cell for expression. Upon expression, some fusion proteins can be isolated or purified from a cell lysate by means of a suitable affinity matrix (see, e.g., Current Protocols in Molecular Biology (Ausubel, F. M. et al., Eds., Vol. 2, Suppl. 26, pp. 16.4.1-16.7.8 (1991)).

The invention relates to a host cell that comprises recombinant nucleic acid(s) encoding an immunoglobulin provided herein (e.g., a humanized immunoglobulin, a humanized light chain or a humanized heavy chain, a mouse immunoglobulin, a mouse light chain or a mouse heavy chain, a chimeric immunoglobulin, a chimeric heavy chain, or a chimeric light chain of the invention). The invention also relates to a host cell that comprises recombinant nucleic acid(s) encoding an antigen-binding portion of the immunoglobulin or their chains. In some embodiments, the host cell comprises a recombinant vector (e.g., expression vector, mammalian cell expression vector) of the invention as referred to herein.

The invention also relates to a method of preparing an immunoglobulin or an immunoglobulin polypeptide chain of this invention. In one embodiment, the method comprises maintaining a host cell of the invention as described herein (e.g., a host cell that contains one or more isolated nucleic acids that encode the immunoglobulin or polypeptide chain (e.g., a light chain and a heavy chain, a light chain only, or a heavy chain only, of the invention) under conditions appropriate for expression of the immunoglobulin or polypeptide chain. For example a host cell can be cultured on a substrate or in suspension. In some embodiments, the method further comprises the step of purifying or isolating the immunoglobulin or polypeptide chain.

The invention further relates to a method of preparing immunoglobulins through phage display. For example, a naïve antibody phage display library on CD52 antigen can be panned. Alternatively, a method of preparing immunoglobulins through guided selection can be used (U.S. Patent Application Publication US 2006-0251658 A1.) A custom library built around, for example, a fixed heavy chain (and/or light chain) CDR3 region of a known anti-CD52 antibody can be created. The CDR1 and CDR2 regions of the heavy and light chains can be derived from a naïve repertiore (Osburn et al., Methods, 36:61-68 (2005)). In one embodiment, anti-CD52 ScFvs can be generated from ScFv naïve antibody libraries which are used to obtain mouse-human chimeric antibodies with the desired binding properties. These libraries may be screened for antibodies with the desired binding properties. ScFv phage libraries may be used. For example, ScFvs which recognize human CD52 can be isolated from scFv guided selection libraries following a series of repeated selection cycles on recombinant human CD52 essentially as described in Vaughan et al. (1996). In brief, following incubation with the library, the immobilized antigen, which is pre-coupled to paramagnetic beads, and bound phage can be recovered by magnetic separation while unbound phage is washed away. Bound phage can then be rescued as described by Vaughan et al. (1996) and the selection process repeated.

In a particular embodiment, a library is constructed consisting of the entire variable domain of the heavy chain of a mouse anti-CD52 antibody fused in a single chain format to a repertoire of naive human light chain variable regions. After selection the pool of human light chain variable regions that complement the mouse heavy chain variable region are identified. A library is then constructed consisting of the repertoire of human light chain variable regions selected above fused in a single chain format to a chimeric heavy chain variable region consisting of naive human CDR1 and CDR2 regions and a fixed CDR3 region from the mouse anti-CD52 antibody heavy chain variable domain. After selection for CD52 binders, the best binding clones are selected. Five of the 6 CDR regions can be human in origin while the CDR-3 of the heavy chain variable region can be identical to the original CDR3 of the mouse heavy chain variable domain.

Selections can be performed using CD52 coupled to DYNABEADS M-270 amine (Dynal) according to the manufacturer's recommendations. Alternatively, selections using biotinylated CD52 can be prepared using the primary amine specific reagent succinimidyl-6-(biotinamido) hexanoate following the manufacturer's instructions (EZ link NHS LC Biotin, Pierce).

Outputs from selections can be tested as periplasmic preparations in high throughput screens based on competition assays which measure the ability of the scFvs present in the periplasmic preparation to compete for binding to CD52.

Samples that are able to compete in the high throughput screens may be subjected to DNA sequencing as described in Vaughan et al. (1996) and Osburn et al. (1996). Clones would then be expressed and purified as scFvs or IgGs and assessed for their ability to bind CD52, neutralize CD52 or a combination thereof, e.g., using assays such as antibody-dependent cell mediated cytotoxicity (ADCC) assay and complement dependent cytotoxicity (CDC) assay. Purified scFv preparations can then be prepared as described in Example 3 of WO 01/66754. Protein concentrations of purified scFv preparations were determined using the BCA method (Pierce). Similar approaches can be used to screen for an optimal partner (the opposite chain) of a fixed immunoglobulin heavy or light chain (or V_(H) or V_(L)).

In a particular embodiment, the invention is directed to a method of producing a hybridoma that secretes a monoclonal antibody that has binding specificity for human CD52 comprising administering lymphocytes of a CD52 transgenic mouse to a non-transgenic mouse having the same strain (e.g., CD1) as the human CD52 transgenic mouse, thereby producing an immunized, non-transgenic mouse. Splenocytes of the immunized, non-transgenic mouse are contacted with immortalized cells, thereby producing fused cells, and the fused cells are maintained under conditions in which hybridomas that secrete a monoclonal antibody having binding specificity for human CD52 are produced, thereby producing a hybridoma that secretes a monoclonal antibody that has binding specificity for human CD52.

Immunoglobulins Containing a Toxin Moiety or Toxin

The invention also relates to immunoglobulins that comprise a toxin moiety or toxin. Suitable toxin moieties comprise a toxin (e.g., surface active toxin, cytotoxin). The toxin moiety or toxin can be linked or conjugated to the immunoglobulin using any suitable method. For example, the toxin moiety or toxin can be covalently bonded to the immunoglobulin directly or through a suitable linker. Suitable linkers can include noncleavable or cleavable linkers, for example, pH cleavable linkers or linkers that comprise a cleavage site for a cellular enzyme (e.g., cellular esterases, cellular proteases such as cathepsin B). Such cleavable linkers can be used to prepare an immunoglobulin that can release a toxin moiety or toxin after the immunoglobulin is internalized.

A variety of methods for linking or conjugating a toxin moiety or toxin to an immunoglobulin can be used. The particular method selected will depend on the toxin moiety or toxin and immunoglobulin to be linked or conjugated. If desired, linkers that contain terminal functional groups can be used to link the immunoglobulin and toxin moiety or toxin. Generally, conjugation is accomplished by reacting toxin moiety or toxin that contains a reactive functional group (or is modified to contain a reactive functional group) with a linker or directly with an immunoglobulin. Covalent bonds are formed by reacting a toxin moiety or toxin that contains (or is modified to contain) a chemical moiety or functional group that can, under appropriate conditions, react with a second chemical group thereby forming a covalent bond. If desired, a suitable reactive chemical group can be added to an immunoglobulin or to a linker using any suitable method. (See, e.g., Hermanson, G. T., Bioconjugate Techniques, Academic Press: San Diego, Calif. (1996).) Many suitable reactive chemical group combinations are known in the art, for example an amine group can react with an electrophilic group such as tosylate, mesylate, halo (chloro, bromo, fluoro, iodo), N-hydroxysuccinimidyl ester (NHS), and the like. Thiols can react with maleimide, iodoacetyl, acrylolyl, pyridyl disulfides, 5-thiol-2-nitrobenzoic acid thiol (TNB-thiol), and the like. An aldehyde functional group can be coupled to amine- or hydrazide-containing molecules, and an azide group can react with a trivalent phosphorous group to form phosphoramidate or phosphorimide linkages. Suitable methods to introduce activating groups into molecules are known in the art (see for example, Hermanson, G. T., Bioconjugate Techniques, Academic Press: San Diego, Calif. (1996)).

Suitable toxin moieties and toxins include, for example, a maytansinoid (e.g., maytansinol, e.g., DM1, DM4), a taxane, a calicheamicin, a duocarmycin, or derivatives thereof. The maytansinoid can be, for example, maytansinol or a maytansinol analogue. Examples of maytansinol analogs include those having a modified aromatic ring (e.g., C-19-decloro, C-20-demethoxy, C-20-acyloxy) and those having modifications at other positions (e.g., C-9-CH, C-14-alkoxymethyl, C-14-hydroxymethyl or aceloxymethyl, C-15-hydroxy/acyloxy, C-15-methoxy, C-18-N-demethyl, 4,5-deoxy). Maytansinol and maytansinol analogs are described, for example, in U.S. Pat. Nos. 5,208,020 and 6,333,410, the contents of which are incorporated herein by reference. Maytansinol can be coupled to antibodies and antibody fragments using, e.g., an N-succinimidyl 3-(2-pyridyldithio)proprionate (also known as N-succinimidyl 4-(2-pyridyldithio)pentanoate (or SPP)), 4-succinimidyl-oxycarbonyl-a-(2-pyridyldithio)-toluene (SMPT), N-succinimidyl-3-(2-pyridyldithio)butyrate (SDPB), 2 iminothiolane, or S-acetylsuccinic anhydride. The taxane can be, for example, a taxol, taxotere, or novel taxane (see, e.g., WO 01/38318). The calicheamicin can be, for example, a bromo-complex calicheamicin (e.g., an alpha, beta or gamma bromo-complex), an iodo-complex calicheamicin (e.g., an alpha, beta or gamma iodo-complex), or analogs and mimics thereof. Bromo-complex calicheamicins include I1-BR, I2-BR, I3-BR, 14-BR, J1-BR, J2-BR and K1-BR. Iodo-complex calicheamicins include I1-I, I2-I, I3-I, J1-I, J2-I, L1-I and K1-BR. Calicheamicin and mutants, analogs and mimics thereof are described, for example, in U.S. Pat. Nos. 4,970,198; 5,264,586; 5,550,246; 5,712,374, and 5,714,586, the contents of each of which are incorporated herein by reference. Duocarmycin analogs (e.g., KW-2189, DC88, DC89 CBI-TMI, and derivatives thereof) are described, for example, in U.S. Pat. Nos. 5,070,092, 5,187,186, 5,641,780, 5,641,780, 4,923,990, and 5,101,038, the contents of each of which are incorporated herein by reference.

Examples of other toxins include, but are not limited to antimetabolites (e.g., methotrexate, 6-mercaptopurine, 6-thioguanine, cytarabine, 5-fluorouracil decarbazine), alkylating agents (e.g., mechlorethamine, thioepa chlorambucil, CC-1065 (see U.S. Pat. Nos. 5,475,092, 5,585,499, 5,846,545), melphalan, carmustine (BSNU) and lomustine (CCNU), cyclophosphamide, busulfan, dibromomannitol, streptozotocin, mitomycin C, and cis-dichlorodiamine platinum (II) (DDP) cisplatin), anthracyclines (e.g., daunorubicin (formerly daunomycin) and doxorubicin), antibiotics (e.g., dactinomycin (formerly actinomycin), bleomycin, mithramycin, mitomycin, puromycin anthramycin (AMC)), duocarmycin and analogs or derivatives thereof, and anti-mitotic agents (e.g., vincristine, vinblastine, taxol, auristatins (e.g., auristatin E) and maytansinoids, and analogs or homologs thereof).

The toxin can also be a surface active toxin, such as a toxin that is a free radical generator (e.g., selenium containing toxin moieties), or radionuclide containing moiety. Suitable radionuclide containing moieties, include for example, moieties that contain radioactive iodine (1311 or 1251), yttrium (90Y), lutetium (177Lu), actinium (225Ac), praseodymium, astatine (211At), rhenium (186Re), bismuth (212Bi or 213Bi), indium (111In), technetium (99mTc), phosphorus (32P), rhodium (188Rh), sulfur (35S), carbon (14C), tritium (3H), chromium (51Cr), chlorine (36C1), cobalt (57Co or 58Co), iron (59Fe), selenium (75Se), or gallium (67Ga).

The toxin can be a protein, polypeptide or peptide, from bacterial sources, e.g., diphtheria toxin, pseudomonas exotoxin (PE) and plant proteins, e.g., the A chain of ricin (RTA), the ribosome inactivating proteins (RIPs) gelonin, pokeweed antiviral protein, saporin, and dodecandron are contemplated for use as toxins.

Antisense compounds of nucleic acids designed to bind, disable, promote degradation or prevent the production of the mRNA responsible for generating a particular target protein can also be used as a toxin. Antisense compounds include antisense RNA or DNA, single or double stranded, oligonucleotides, or their analogs, which can hybridize specifically to individual mRNA species and prevent transcription and/or RNA processing of the mRNA species and/or translation of the encoded polypeptide and thereby effect a reduction in the amount of the respective encoded polypeptide. Ching, et al., Proc. Natl. Acad. Sci. U.S.A. 86: 10006-10010 (1989); Broder, et al., Ann. Int. Med. 113: 604-618 (1990); Loreau, et al., FEBS Letters 274: 53-56 (1990). Useful antisense therapeutics include for example: Veglin™ (VasGene) and OGX-011 (Oncogenix).

Toxins can also be photoactive agents. Suitable photoactive agents include porphyrin-based materials such as porfimer sodium, the green porphyrins, chlorin E6, hematoporphyrin derivative itself, phthalocyanines, etiopurpurins, texaphrin, and the like.

The toxin can be an antibody or antibody fragment that binds an intracellular target. Such antibodies or antibody fragments can be directed to defined subcellular compartments or targets. For example, the antibodies or antibody fragments can bind an intracellular target selected from erbB2, EGFR, BCR-ABL, p21Ras, Caspase3, Caspase7, Bcl-2, p53, Cyclin E, ATF-1/CREB, HPV16 E7, HP1, Type IV collagenases, cathepsin L as well as others described in Kontermann, R. E., Methods, 34:163-170 (2004), incorporated herein by reference in its entirety.

Therapeutic Methods and Compositions

The antibodies of this invention are useful in immuno-suppression and immuno-ablation. The antibodies target CD52-expressing cells (e.g., T and B cells) and reduce (or “deplete” as used herein) their population in a subject in need thereof. Lymphocyte depletion may be useful in treating a variety of diseases and conditions such as inflammation, autoimmune diseases and cancer (e.g., lymphocyte (either B or T cell) malignancy). See, e.g., Reiff, A., Hematology, 10(2): 79-93 (2005). Examples of diseases and conditions that can be treated with the antibodies or antigen-binding portions of this invention include, without limitation, multiple sclerosis, lupus, rheumatoid arthritis, graft versus host disease (GVHD), inflammatory bowl disease, vasculitis, Behcet's disease, Wegener's granulomatosis, Sjogren's syndrome, uveitis, psoriasis, scleroderma, polymyositis, type I (autoimmune-based) diabetes, autoimmune cytopenias (e.g., autoimmune neutropenia, transfusion-dependent refractory PRCA, leukemia and lymphoma such as non-Hodgkin's lymphoma with bulky disease and B-cell chronic lymphocytic leukemia.

Accordingly, aspects of this invention are methods for lymphocyte depletion, and for treating inflammation, an autoimmune disease or cancer by administering an effective amount of an antibody of the invention to a subject in need thereof (e.g., a human patient having an autoimmune disease, a blood cancer, or a patient who is to receive a transplantation). The antibody also can be administered prophylactically to prevent onset of inflammation or relapse of an autoimmune disease or cancer. For example, the antibody of this invention can be administered as part of a conditioning regimen to prepare a patient for a transplantation (e.g., a stem cell transplant, an infusion of autologous of allogeneic T cells, or a solid organ transplant).

Some anti-CD52 antibodies of this invention preferentially target certain populations of CD52+ cells. One possible explanation is that epitopes to which these antibodies bind include one or more carbohydrate groups on the CD52 protein, and such carbohydrate groups may be more prevalent on CD52 expressed on one cell type versus another. For example, we have found that antibody 7F11, 5F7, 3G7, and 11C11 deplete T cells to a greater extent than B cells. Thus, the humanized and chimeric versions of these antibodies may be used to treat T cell malignancy with milder immunosuppressing side effects.

Because antibodies of this invention target CD52-expressing cells, the antibodies also can be used to deplete CD52+ cell types other than T cells and B cells. For example, studies have shown that vascular leukocytes (VLC) and Tie2+ monocytes-myeloid cells expressing high levels of CD52− promote tumor angiogenesis and contribute to tumor resistance to anti-VEGF therapy. Pulaski et al., J. Translational Med. 7:49 (2009). Anti-CD52 antibodies of this invention thus can be used to inhibit tumor angiogenesis by targeting VLC and Tie2+ monocytes. For this purpose, the anti-CD52 antibodies can be administered systemically, or locally at a site of neovascularization, such as a tumor site. Anti-CD52 antibody therapy can be used in conjunction with standard-of-care cancer treatment such as chemotherapy, surgery, or radiation, or with another targeted therapy such as anti-VEGF antibody therapy. Anti-CD52 antibody therapy can be used to treat, for example, breast cancer, lung cancer, glioma, colorectal cancer, and any other indications of anti-VEGF antibodies. Anti-CD52 antibody therapy also can be used in other neovascularization conditions including non-oncological neovascular conditions.

Antibodies of this invention can be administered to an individual (e.g., a human) alone or in conjunction with another agent (e.g., an immunosuppressant) in a combination therapy. The antibody can be administered before, along with or subsequent to administration of the additional agent. In some embodiments, the additional agent is, for example, an anti-inflammatory compound such as sulfasalazine, another non-steroidal anti-inflammatory compound, or a steroidal anti-inflammatory compound. In some embodiments, the additional agent is another lympho-depleting antibody such as another anti-CD52 antibody, an anti-CD20 antibody, an anti-BAFF antibody, an anti-BAFF-R antibody, and the like. In some embodiments, the additional agent is, e.g., a cytokine (e.g., IL-7), anti-cytokine receptor antibody, or a soluble receptor, that skews, manipulates, and/or augments the reconstitution process that occurs following lymphodepletion mediated by an anti-CD52 antibody (see, e.g., Sportes et al., “ ”Cytokine Therapies: Ann. N.Y. Acad. Sci. 1182:28-38 (2009)). In another embodiment, a synthetic peptide mimetic can be administered in conjunction with an immunoglobulin of the present invention.

Studies have shown that lymphocyte depletion by alemtuzumab is mediated by neutrophils and NK cells (Hu et al., Immunology 128:260-270 (2009). Thus, in an embodiment of combination therapy, an agent that stimulates neutrophils and NK cells can be administered to a patient, before, during or after anti-CD52 antibody therapy, to augment the antibody therapy. Stimulating neutrophils and/or NK cells include, without limitation, (1) increasing their rates of division, (2) increasing their cell surface expression of the Fc receptors corresponding to the isotype of the anti-CD52 antibody (e.g., FcγRIIIa and FcγRIIIb, FcγRII, FcγRI, and FcαRI), (3) mobilizing and increasing the number of circulating cells, (4) recruiting the cells to target sites (e.g., sites of tumors, inflammation, or tissue damage), (5) and increasing their cytotoxic activity. Examples of agents that stimulate neutrophils and/or NK cells include, for example, granulocyte monocyte colony stimulating factor (GM-CSF) (e.g., LEUKINE® or sargramostim and molgramostim); granulocyte colony stimulating factor (G-CSF) (e.g., NEUPOGEN® or filgrastim, pegylated filgrastim, and lenograstim); interferon gamma (e.g., ACTIMMUNE®); CXC chemokine receptor 4 (CXCR4) antagonists (e.g., MOZOBIL™ or plerixafor); and CXC chemokine receptor 2 (CXCR2) agonists. The neutrophil count of the patient may be monitored periodically to ensure optimal treatment efficacy. The neutrophil count of the patient also can be measured prior to the start of the anti-CD52 antibody treatment. The stimulator's amount can be adjusted based on the patient's neutrophil count. A higher dose of the stimulator may be used if the patient has a lower than normal neutrophil count. During periods of neutropenia, which may be caused by treatment with the anti-CD52 antibody, a higher dose of the neutrophil stimulator may also be administered to maximize the effect of the anti-CD52 antibody.

Because neutrophil and/or NK stimulation improves the efficacy of anti-CD52 antibody therapy, this embodiment of combination therapy allows one to use less antibody in a patient while maintaining similar treatment efficacy. Using less anti-CD52 antibody while maintaining treatment efficacy may help reduce side effects of the anti-CD52 antibody, which include immune response in the patient against the administered antibody as well as development of secondary autoimmunity (autoimmunity that arises during or after anti-CD52 antibody treatment). This embodiment of combination of therapy is also useful in an oncology setting, e.g., when the patient has neutropenia.

In another embodiment of combination therapy, one can use a stimulator of regulatory T cells to augment anti-CD52 antibody therapy. Our data show that anti-CD52 antibodies deplete CD4⁺CD25⁺FoxP3⁺ regulatory T cells to a much lesser extent as compared to other CD4⁺ T cells. Regulatory T cells (also known as “Treg” or suppressor T cells) are cells that are capable of inhibiting the proliferation and/or function of other lymphoid cells via contact-dependent or contact-independent (e.g., cytokine production) mechanisms. Several types of regulatory T cells have been described, including γδ T cells, natural killer T (NKT) cells, CD8⁺T cells, CD4⁺T cells, and double negative CD4⁻CD8⁻T cells. See, e.g., Bach et al., Immunol. 3:189-98 (2003). CD4⁺CD25⁺FoxP3⁺ regulatory T cells have been referred as “naturally occurring” regulatory T cells; they express CD4, CD25 and forkhead family transcription factor FoxP3 (forkhead box p3). Thus, in this embodiment of combination therapy, one can administer an agent that stimulates CD4⁺CD25⁺FoxP3⁺ regulatory T cells before, during or after the anti-CD52 antibody therapy, to skew the composition of the immune system following lympho-depletion. The agent may, for example, activate those T cells, stabilize and/or expand the population of the cells, mobilize and increase circulation of the cells, and/or recruit the cells to target sites. Examples of such agents are rapamycin, active or latent TGF-β (e.g., TGF-β1, TGF-β2, TGF-β3, TGF-β4, and TGF-β5), IL-10, IL-4, IFN-α, vitamin D3, dexamethasone, and mycophenolate mofetil (see, e.g., Barrat et al., J Exp. Med. 195:603-616 (2002); Gregori et al., J Immunol. 167: 1945-1953 (2001); Battaglia et al., Blood 105: 4743-4748 (2005); Battaglia et al., J Immunol. 177:8338-8347 (2006)).

In this invention, an effective amount of anti-CD52 antibody for treating a disease is an amount that helps the treated subject to reach one or more desired clinical end points. For example, for lupus (whose manifestations include systemic lupus erythematosus, lupus nephritis, cutaneous lupus erythematosus, CNS lupus, cardiovascular manifestations, pulmonary manifestations, hepatic manifestations, haematological manifestations, gastrointestinal manifestations, musculoskeletal manifestations, neonatal lupus erythematosus, childhood systemic lupus erythematosus, drug-induced lupus erythematosus, anti-phospholipid syndrome, and complement deficiency syndromes resulting in lupus manifestations; see, e.g., Robert G. Lahita, Editor, Systemic Lupus Erythematosus, 4th Ed., Elsevier Academic Press, 2004), clinical endpoints can be measured by monitoring of an affected organ system (e.g., hematuria and/or proteinuria for lupus nephritis) and/or using a disease activity index that provides a composite score of disease severity across several organ systems (e.g., BILAG, SLAM, SLEDAI, ECLAM). See, e.g., Mandl et al., “Monitoring patients with systemic lupus erythematosus” in Systemic Lupus Erythematosus, 4^(th) edition, pp. 619-631, R. G. Lahita, Editor, Elsevier Academic Press, (2004).

In another example of autoimmune disease, multiple sclerosis (including relapsing-remitting, secondary progressive, primary progressive, and progressive relapsing multiple sclerosis ((Lublin et al., Neurology 46 (4), 907-11 (1996)), diagnosed is made by, for example, the history of symptoms and neurological examination with the help of tests such as magnetic resonance imaging (MRI), spinal taps, evoked potential tests, and laboratory analysis of blood samples. In MS, the goal of treatment is to reduce the frequency and severity of relapses, prevent disability arising from disease progression, and promote tissue repair (Compston and Coles, 2008). Thus, an amount of anti-CD52 antibody that helps achieve a clinical endpoint consistent with that goal is an effective amount of antibody for the treatment.

To minimize immunogenicity, it is preferred that a humanized antibody be used to treat a human patient in therapeutic methods and compositions of this invention. In cases where repeated administration is not necessary, it may also be appropriate to administer a mouse:human chimeric antibody of this invention to a human patient.

The antibodies of the invention can be used to treat an individual who has previously been treated with Campath-1H® who has developed neutralizing antibodies to Campath-1H® (e.g., a Campath-1H®-refractory individual). For example, one could treat an individual having an autoimmune disease (e.g., multiple sclerosis, lupus, vasculitis) and/or a cancer (e.g., a leukemia (e.g., chronic lymphocytic leukemia), a lymphoma (e.g., non-Hodgkin's lymphoma)) who has previously been treated with Campath-1H® (e.g., with one or more courses of Campath-1H® treatment) and who has developed neutralizing antibodies to Campath-1H® that reduce the efficacy of further Campath-1H® treatment. We have shown that the humanized antibodies of this invention (e.g., humanized 2C3, 12G6, and 9D9) can bind to human CD52 despite the presence of neutralizing antibodies to alemtuzumab. In another embodiment, one could treat an individual who had become refractory to treatment with a particular humanized antibody described herein with one of the other humanized antibodies described herein.

The antibody of this invention can be administered in a single unit dose or multiple doses at any time point deemed appropriate by a health care provider. The dosage can be determined by methods known in the art and can be dependent, for example, upon the individual's age, sensitivity, tolerance and overall well-being. A variety of routes of administration can be used, including, but not necessarily limited to, parenteral (e.g., intravenous, intraarterial, intramuscular, intrathecal, intraperitoneal, subcutaneous injection), oral (e.g., dietary), locally, topical, inhalation (e.g., intrabronchial, intranasal or oral inhalation, intranasal drops), or rectal, depending on the disease or condition to be treated. Parenteral administration may be one preferred mode of administration.

In one embodiment, the antibodies of the invention are administered to a patient using the same dosing regimen as Campath-1H® (e.g., the dosing regimen of Campath-1H® for chronic lymphocytic leukemia). In another embodiment, an antibody of the invention is administered to a patient having an autoimmune disease (e.g., multiple sclerosis (MS)) in a regimen comprising administration of a first cycle of the antibody followed by at least one further cycle of the antibody, in which each treatment cycle comprises 1-5 doses that are applied on consecutive days, and wherein each treatment cycle is separated from the next cycle by at least 1-24 months (e.g., 12 months). For example, in one embodiment, a patient having multiple sclerosis is treated with a first cycle of the antibody comprising 5 daily doses of the antibody followed by at least one further cycle of antibody treatment, in which the treatment occurs 12 months after the first cycle and comprises 3 doses of the antibody applied on consecutive days. In another embodiment, a patients having MS is only re-treated once evidence of renewed MS activity has been observed (see, e.g., WO 2008/031626; the teachings of which are incorporated herein by reference in their entirety). In some embodiments, it may be necessary to administer more frequent courses of treatment (e.g., every four months, every six months) if patients with more advanced forms of MS or more progressive forms of other autoimmune diseases (such as vasculitis; see, e.g., Walsh et al., Ann Rheum Dis 67:1322-1327 (2008)) experience a relapse early on after their last course of treatment. Evidence of renewed MS activity may be determined based on the professional judgment of the treating clinician, using any means that may be available to such clinician. A variety of techniques are currently available to clinicians to diagnose renewed MS activity including, without limitation, by clinical means (relapse or progression of neurological disability) or by magnetic resonance imaging (MRI) of the brain or spinal cord. As is well understood by medical practitioners, disease activity detected via MRI may be indicated by the occurrence of new cerebral or spinal lesions on T1 (enhanced or non-enhanced)- or T2-weighted images or by the increase of the volume of such lesions. As diagnostic methods for MS are continually evolving, it is anticipated there may be additional methods in the future that will detect renewed MS activity (e.g., magnetization transfer ratio or MR-spectroscopy). The particular diagnostic method used to detect renewed MS activity is not a limitation of the claimed invention. In certain embodiments, repeated MRIs are performed in fixed intervals after a treatment cycle in order to determine whether re-treatment of any given patient is necessary and the optimal time point for re-treatment of such patient. In general, it is desirable for re-treatment to occur before the disease re-manifests clinically.

Formulation will vary according to the route of administration selected (e.g., solution, emulsion). An appropriate composition comprising the antibody to be administered can be prepared in a physiologically acceptable vehicle or carrier. The composition can comprise multiple doses or be a single unit dose composition. For solutions or emulsions, suitable carriers include, for example, aqueous or alcoholic/aqueous solutions, emulsions or suspensions, including saline and buffered media. Parenteral vehicles can include sodium chloride solution, Ringer's dextrose, dextrose and sodium chloride, lactated Ringer's or fixed oils. Intravenous vehicles can include various additives, preservatives, or fluid, nutrient or electrolyte replenishers (See, generally, Remington's Pharmaceutical Sciences, 17th Edition, Mack Publishing Co., PA, 1985). For inhalation, the compound can be solubilized and loaded into a suitable dispenser for administration (e.g., an atomizer, nebulizer or pressurized aerosol dispenser).

Diagnostic Methods and Compositions

The immunoglobulins of the present invention also are useful in a variety of processes with applications in research and diagnosis. For instance, they can be used to detect, isolate, and/or purify human CD52 or variants thereof (e.g., by affinity purification or other suitable methods such as flow cytometry, e.g., for cells, such as lymphocytes, in suspension), and to study human CD52 structure (e.g., conformation) and function. For in vitro applications, wherein immunogenicity of the antibody is not a concern, the mouse and chimeric antibodies of this invention will be useful in addition to humanized antibodies.

The immunoglobulins of the present invention can be used in diagnostic applications (e.g., in vitro, ex vivo). For example, the humanized immunoglobulins of the present invention can be used to detect and/or measure the level of human CD52 in a sample (e.g., on cells expressing human CD52 in tissues or body fluids, such as an inflammatory exudate, blood, serum, bowel fluid, tissues bearing human CD52). A sample (e.g., tissue and/or body fluid) can be obtained from an individual and an immunoglobulin described herein can be used in a suitable immunological method to detect and/or measure human CD52 expression, including methods such as flow cytometry (e.g., for cells in suspension such as lymphocytes), enzyme-linked immunosorbent assays (ELISA), including chemiluminescence assays, radioimmunoassay, and immunohistology.

In one embodiment, a method of detecting human CD52 in a sample is provided, comprising contacting a sample with an immunoglobulin of the present invention under conditions suitable for specific binding of the immunoglobulin to human CD52 and detecting antibody-CD52 complexes which are formed. In an application of the method, the immunoglobulins described herein can be used to analyze normal versus inflamed tissues (e.g., from a human) for human CD52 reactivity and/or expression (e.g., immunohistologically) to detect associations between e.g., inflammatory bowel disease (IBD), autoimmune diseases (such as multiple sclerosis and lupus), cancer (such as non-Hodgkin's lymphoma and chronic lymphocytic leukemia), or other conditions and increased expression of human CD52 (e.g., in affected tissues). Thus, the immunoglobulins of the present invention permit immunological methods of assessment of the presence of human CD52 in normal and inflamed tissues, through which the presence of disease, disease progress and/or the efficacy of anti-human CD52 therapy in the treatment of disease, e.g., inflammatory disease can be assessed.

In addition, the immunoglobulins can be used to examine tissues after treatment with a depleting anti-CD52 therapeutic antibody to gauge how effective the depletion has been as well as to determine whether there has been any downregulation in the expression of CD52 (Rawstrom et al., Br. J. Heam., 107:148-153 (1999)).

Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Exemplary methods and materials are described below, although methods and materials similar or equivalent to those described herein can also be used in the practice or testing of the present invention. All publications and other references mentioned herein are incorporated by reference in their entirety. In case of conflict, the present specification, including definitions, will control. Although a number of documents are cited herein, this citation does not constitute an admission that any of these documents forms part of the common general knowledge in the art. Throughout this specification and claims, the word “comprise,” or variations such as “comprises” or “comprising” will be understood to imply the inclusion of a stated integer or group of integers but not the exclusion of any other integer or group of integers. The materials, methods, and examples are illustrative only and not intended to be limiting.

EXEMPLIFICATION Example 1: Generation of Mouse Anti-Human CD52 Antibodies

The mouse anti-human CD52 antibodies in the following working examples were generated by immunizing CD1 strain mice with splenocytes from human CD52 transgenic mice with a CD1 background (FIG. 1A), where display of human CD52 on the surface of mouse B and T cells of the transgenic mice was verified by flow cytometry. Because the transgenic mice had the same background (CD1) as the immunized mice, splenocytes from the transgenic mice presented human CD52 at the cell surface as a unique, non-self antigen in a native format, and the immunized nontransgenic mice mounted an antibody response primarily towards the human CD52.

To collect splenocytes from the human CD52 transgenic mice, the mice were euthanized, spleens were harvested and single cell suspensions were prepared by passing through a syringe. CD1 mice were then immunized with the collected human CD52 positive spleen cells at 5×10⁶ in 100 μl per mouse with or without Freund's Complete Adjuvant by intraperitoneal (i.p.) injection. Mice were given two booster doses every two weeks after first immunization with transgenic mouse human CD52 positive spleen cells at 5×10⁶ in 100 μl per mouse with Freund's Incomplete Adjuvant, ip.

Eye bleeds were collected 100-200 μl per mouse in yellow-capped serum separator tubes from all mice before immunization to determine base level reactivity, and a week after every round of immunization to determine base level reactivity, and a week after every round of immunization to determine anti-human CD52 specific immune response. Mice that mounted high levels of anti-human CD52 reactivity as measured by FACS on CHO K1 cells engineered to express human CD52 protein, but not on parental CHO K1 cells were sacrificed, blood was harvested and spleens were collected under sterile conditions to generate hybridomas. Hybridomas were generated by using a non-secreting mouse myeloma cell-line SP2/0 Ag14 or NS1 myeloma cells as fusion partners 3-4 days post immunization. Fused cells were placed in complete growth medium containing hypoxanthine, aminopterin and thymidine to generate hybridomas. After screening many hybridoma supernatants, several clones were selected that produced specific anti-human CD52 antibodies and were further subcloned to derive a clonal population. Hybridoma clones that produced anti-human CD52 antibodies were scaled up for further development.

Example 2: PCR Analysis of Heavy and Light Chains of Mouse Anti-Human CD52 Antibodies

A number of mouse anti-human CD52 monoclonal antibodies (FIG. 1B) were identified by testing hybridoma supernatants for the presence of anti-human CD52 reactivity. Individual clones were selected and the mouse heavy and light chain variable sequences were identified by PCR cloning and sequencing. The sequences of the light chains are shown in FIG. 2 as compared to YTH 34.5 HL (i.e., Campath IG Kappa (rat) and a reagent antibody CF1D12 (CF1D12 Kappa) (Invitrogen Life Science Technologies). Similarly, the sequences of the heavy chains are shown in FIG. 3 as compared to YTH 34.5 HL and a reagent antibody CF1D12.

A total of 10 Zunique light chain variable sequences and 11 unique heavy chain variable sequences were identified. If one includes Campath® and CF1D12, 7 unique CDR-1 regions (Table 1), 8 unique CDR-2 regions (Table 2) and 7 unique CDR-3 regions (Table 3) were identified within the light chains of anti-human CD52 antibodies.

TABLE 1 Light Chain CDR-1 Sequences Light Chain CDR-1 Sequence A KASQNIDKYLN (SEQ ID NO: 27) B KSSQSLLESDGRTYLN (SEQ ID NO: 28) C KSSQSLLDSDGKTYLN (SEQ ID NO: 29) D KSSQSLLDSDGRTYLN (SEQ ID NO: 30) E KSSQSLLYSNGKTYLN (SEQ ID NO: 31) F RSSQSLVHTNGNSYLH (SEQ ID NO: 32) G RSSQSLVHTNGNTYLH (SEQ ID NO: 33)

TABLE 2 Light Chain CDR-2 Sequences Light Chain CDR-2 Sequence A NTNNLQT (SEQ ID NO: 34) B LVSNLDS (SEQ ID NO: 35) C LVSKLDS (SEQ ID NO: 36) D LVSNLGS (SEQ ID NO: 37) E LVSALDS (SEQ ID NO: 38) F LVSNLNS (SEQ ID NO: 39) G LVSHLDS (SEQ ID NO: 40) H MVSNRFS (SEQ ID NO: 41)

TABLE 3 Light Chain CDR-3 Sequences Light Chain CDR-3 Sequence A LQHISRPRT (SEQ ID NO: 42) B WQGTHFPWT (SEQ ID NO: 43) C VQGSHFHT (SEQ ID NO: 44) D VQGTRFHT (SEQ ID NO: 45) E VQGTHLHT (SEQ ID NO: 46) F SQSTHVPFT (SEQ ID NO: 47) G SQSAHVPPLT (SEQ ID NO: 48)

If one includes Campath® and CF1D12, a total of 8 unique CDR-1 regions (Table 4), 10 unique CDR-2 regions (Table 5) and 8 unique CDR-3 regions (Table 6) have been identified within the heavy chains of anti-human CD52 antibodies.

TABLE 4 Heavy Chain CDR-1 Sequences Heavy Chain CDR-1 Sequence A GFTFTDFYMN (SEQ ID NO: 49) B GFTFSDAWMD (SEQ ID NO: 50) C RFTFSDAWMD (SEQ ID NO: 51) D GLTFSDAWMD (SEQ ID NO: 52) E GFPFSNYWMN (SEQ ID NO: 53) F GFTFNKYWMN (SEQ ID NO: 54) G GFTFNTYWMN (SEQ ID NO: 55) H GFTFTDYYMS (SEQ ID NO: 56)

TABLE 5 Heavy Chain CDR-2 Sequences Heavy Chain CDR-2 Sequence A FIRDKAKGYTTEYNPSVKG (SEQ ID NO: 57) B EIRNKAKNHVAYYAESVKG (SEQ ID NO: 58) C EIRNKANNHATYYAESVKG (SEQ ID NO: 59) D EIRNKAKNHVKYYAESVKG (SEQ ID NO: 60) E EIRNKAKNHATYYAESVKG (SEQ ID NO: 61) F EIRKKVNNHATYYAESVKG (SEQ ID NO: 62) G QIRLKSNNYATHYAESVKG (SEQ ID NO: 63) H QIRLKSDNYATHYAESVKG (SEQ ID NO: 64) I FIRNKANGYTTEYNASVKG (SEQ ID NO: 65) J FIRNKANGYTTEYSASVKG (SEQ ID NO: 66)

TABLE 6 Heavy Chain CDR-3 Sequences Heavy Chain CDR-3 Sequence A AREGHTAAPFDY (SEQ ID NO: 67) B TTLDS (SEQ ID NO: 68) C TSLDY (SEQ ID NO: 69) D TGLDY (SEQ ID NO;70) E TPIDY (SEQ ID NO: 71) F TPVDF (SEQ ID NO: 72) G TRYIFFDY (SEQ ID NO: 73) H TRYIWFDY (SEQ ID NO: 74)

The association of specific light and heavy chain CDR regions within 13 different anti-human CD52 antibodies is depicted in Table 7.

TABLE 7 Classification of Anti-Human CD52 Antibodies on the Basis of CDR Composition Clone Heavy Chain CDR-1 Light Chain Name CDR-1 CDR-2 CDR-3 CDR-1 CDR-2 CDR-3 Campath A A A A A A CF1D12 B B B B B B 8G3.25.3.5 C C C C C B GMA 4G7.F3 B D C C D B GMA 9D9.A2 B E B C E B GMA B E C C C B 11C11.C5 GMA 3G7.E9 B F C C F B 5F7.1.1.4 D E D D G B 12G6.15.1.2 E G E E C C 23E6.2.2.1 F H E E C D 2C3.3.8.1 G G F E C E 7F11.1.9.7 H I G F H F 4B10.1.2.4 H J H G H G Clones 8G3.25.3.5, 4G7.F3, 9D9.A2, 11C11.C5, 3G7.E9, 5F7.1.1.4, 12G6.15.1.2, 23E6.2.2.1, 2C3.3.8.1, 7F11.1.9.7 and 4B10.1.2.4 are hereafter referred to as 8G3, 4G7, 9D9, 11C11, 3G7, 5F7, 12G6, 23E6, 2C3, 7F11 and 4B10, respectively.

TABLE 7.1 SEQ ID NOs of the CDRs of the Anti-Human CD52 Antibodies Clone Heavy Chain Light Chain Name CDR-1 CDR-2 CDR-3 CDR-1 CDR-2 CDR-3 Campath 49 57 67 27 34 42 CF1D12 50 58 68 28 35 43 8G3 51 59 69 29 36 43 4G7 50 60 69 29 37 43 9D9 50 61 68 29 38 43 11C11 50 61 69 29 36 43 3G7 50 62 69 29 39 43 5F7 52 61 70 30 40 43 12G6 53 63 71 31 36 44 23E6 54 64 71 31 36 45 2C3 55 63 72 31 36 46 7F11 56 65 73 32 41 47 4B10 56 66 74 33 41 48

Example 3: Cloning of Mouse IgG Variable Region Genes from Mouse Hybridoma Cells to Generate a Mouse/Human Chimeric IgG1 Antibody

Actively proliferating and antibody secreting hybridoma cells were used to isolate RNA using Trizol reagent (Gibco/BRL) following the manufacturer's suggested protocol. RNA was quantified by measuring OD using Nanodrop, and the integrity of the RNA was determined by running it on a gel or by using a bioanalyzer. Total RNA was reverse transcribed to cDNA and the variable regions for the heavy and light chains were amplified by polymerase chain reaction (PCR). The cDNA was generated using BD Sprint PowerScript Reverse Transcriptase (Clontech) and Oligo(dT) primer at 0.5 μg/μl (Invitrogen Cat # Y01212) and reverse primers (located in the constant region of the heavy and light chains) listed numerically below at 10 μM following the manufacturer's protocol. Specifically, primers numbered 3 (SEQ ID NO: 77), 11 (SEQ ID NO: 85), 19 (SEQ ID NO: 93), 20 (SEQ ID NO: 94) and 21 (SEQ ID NO: 95) were employed. PCR amplification of the heavy and light chain variable regions was carried out using cDNA generated as described above. 1 μl of cDNA was mixed with forward primer and reverse primers at 10 μM each for both heavy and light chains and mixed with PCR super mix (Invitrogen) in the presence of 2 μl of MgCl₂ at 25 mM. The PCR program was run in the following steps: 1) 95° C. for 2 minutes; 2) 95° C. for 30 seconds; 3) 56° C. for 30 seconds; 4) 68° C. for 45 seconds; 5) Repeat steps 2 to 4 25 times; 6) 68° C. for 10 minutes and hold at 16° C. The PCR product was analyzed on a 2% gel for the presence of variable region sequence product of about 300-400 bp in size and the appropriate bands were cloned into pCR2.1-TOPO TA cloning Kit (Invitrogen) following the manufacturer's instructions and the cloned and sequence confirmed using M13 primers. Primers used for reverse transcribing and for PCR amplification of light chain and heavy chain sequences are provided:

Light chain primers 1) Lead-ML kappa = (SEQ ID NO: 75) 5′ ATGGGCWTCAARATGRARWCWCAT 3′ (Forward primer in leader sequence) 2) FR1-ML kappa = (SEQ ID NO: 76) 5′ GAYATTGTGMTRACMCARKMTCAA 3′ (Forward primer in the frame work 1) 3) ML kappa const = (SEQ ID NO: 77) 5′ ACTGGATGGTGGGAAGATGGA 3′(Reverse primer in constant region) 4) VK-MK = (SEQ ID NO: 78) 5′ GAYATTGTGMTSACMCARWCTMCA 3′ (Forward primer in the frame work 1) 5) MKC-Const = (SEQ ID NO: 79) 5′ GGATACAGTTGGTGCAGCATC 3′ (Reverse primer in constant region) Heavy chain primers 6) MH-SP-ALT1 = (SEQ ID NO: 80) 5′ ATGRASTTSKGGYTMARCTKGRTT 3′ (Forward primer in leader sequence) 7) MH-SP-ALT2 = (SEQ ID NO: 81) 5′ ATGRAATGSASCTGGGTYWTYCTCT 3′ (Forward primer in leader sequence) 8) MH-FR1 = (SEQ ID NO: 82) 5′ SAGGTSMARCTGCAGSAGTCT 3′ (Forward primer in the frame work 1) 9) MH-FR1-1 = (SEQ ID NO: 83) 5′ SAGGTGMAGCTCSWRSARYCSGGG 3′ (Forward primer in the frame work 1) 10) MH-J2 = (SEQ ID NO: 84) 5′ TGAGGAGACTGTGAGAGTGGTGCC 3′ (Reverse primer in J region) 11) MH-gamma-const = (SEQ ID NO: 85) 5′ AYCTCCACACACAGGRRCCAGTGGATAGAC 3′ (Reverse primer in constant region) 12) VH MH1 = (SEQ ID NO: 86) 5′ SARGTNMAGCTGSAGSAGTC 3′ (Forward primer in the frame work 1) 13) VH MH2 = (SEQ ID NO: 87) 5′ SARGTNMAGCTGSAGSAGTCWGG 3′ (Forward primer in the frame work 1) 14) VH MH3 = (SEQ ID NO: 88) 5′ CAGGTTACTCTGAAAGWGTSTG 3′ (Forward primer in the frame work 1) 15) VH MH4 = (SEQ ID NO: 89) 5′ GAGGTCCARCTGCAACARTC 3′(Forward primer in the frame work 1) 16) VH MH5 = (SEQ ID NO: 90) 5′ CAGGTCCAACTVCAGCARCC 3′(Forward primer in the frame work 1) 17) VH MH6 = (SEQ ID NO: 91) 5′ GAGGTGAASSTGGTGGAATC 3′(Forward primer in the frame work 1) 18) VH MH7 = (SEQ ID NO: 92) 5′ GATGTGAACTTGGAAGTGTC 3′(Forward primer in the frame work 1) 19) IgG1 = (SEQ ID NO: 93) 5′ ATAGACAGATGGGGGTGTCGTTTTGGC 3′ (Reverse primer in mouse IgG1 CH1 constant region) 20) IgG2A = (SEQ ID NO: 94) 5′ CTTGACCAGGCATCCTAGAGTCA 3′ (Reverse primer in mouse IgG2A CH1 constant region) 21) IgG2B = (SEQ ID NO: 95) 5′ AGGGGCCAGTGGATAGAGTGATGG 3′ (Reverse primer in mouse IgG2B CH1 constant region)

Degenerate primers led to some degeneracy in the 5′ end of the frame work 1 region of both heavy and light chains. The consensus DNA sequence from several independent heavy chain variable region clones and from light chain variable region clones was used to derive the amino acid sequence.

Functional chimeric anti-CD52 antibodies were produced by joining the heavy chain and light chain variable regions to the DNA encoding human IgG1 heavy chain (identical sequence to that found in Campath-1H®) and human kappa light chain constant region (identical sequence to that found in Campath-1H®), respectively. To generate pCEP4 (Invitrogen) light chain vector encoding CD52 antibody light chain, the light chain variable sequence was PCR amplified and engineered by ligase independent cloning into the pCEP4 LIC light chain vector to have the human kappa signal sequence in the 5′ end and the light chain constant region in the 3′end. Similarly, to generate pCEP4 heavy chain vector, the variable region of the heavy chain sequence was engineered by ligase independent cloning into the pCEP4 LIC heavy chain vector to have the human kappa chain signal sequence in the 5′ end and the heavy chain constant region encompassing CH1, hinge, CH2 and CH3 regions in the 3′end. The constant region amino acid sequences for both heavy and light chains are identical to that of the constant regions present in Campath1H antibody.

Briefly, pCEP4 LIC vector was digested with BfuA1 (New England Biolabs-NEB) in appropriate buffer following the manufacturer's recommendations and after complete digestion, the vector was purified using PureLink PCR Purification Kit (Invitrogen). The linearized plasmid was then treated with T4 DNA polymerase (New England Biolabs) to generate single-stranded ends and was used to clone the variable region fragment. Heavy chain specific pCEP4 LIC vector was used for cloning heavy chain variable region and light chain specific pCEP4 LIC vector was used for cloning light chain variable region. Variable region insert was generated by PCR using pCR2.1-TOPO heavy chain variable region containing plasmid or pCR2.1-TOPO light chain variable region containing plasmid as template and primers that contain variable chain specific sequence and vector overhangs. VENT DNA polymerase (New England Biolabs) was used for PCR amplification of the insert. PCR-amplified insert was gel purified and treated with T4 DNA polymerase to generate single-stranded ends. Prepared vectors for heavy chain and light chain and respective variable region insert fragments were combined and incubated at room temperature for 10 minutes and used to transform TOPO10 cells (Invitrogen), ampicillin resistant colonies were picked and sequence verified. pCEP4 heavy chain and pCEP4 light chain clones that had the correct heavy chain and light chain sequences inserted in-frame were amplified and used for protein production. The heavy chain construct was co-transfected with the corresponding light chain construct in a 1:1 ratio into HEK293 cells (Invitrogen) using the cationic lipid Lipofectamine™ 2000 (Invitrogen). The conditioned medium was harvested three days after the transfection and the chimeric antibody was purified using protein A chromatography. For this chromatography method, the medium was added to protein A and washed with 50 column volumes of PBS. The chimeric antibody was eluted with 5 column volumes of 12.5 mM citric acid, pH 3.0. The pH of the eluted antibody was neutralized by addition of 0.5 M HEPES. The buffer was exchanged into PBS by using a PD-10 gel filtration column.

Example 4: Analysis of the Epitope Specificities of Chimeric Anti-Human CD52 Monoclonal Antibodies

The epitope specificities of the clones were determined by assessing the ability of the chimeric antibodies to bind to a panel of cell lines engineered to express mutants of human CD52 (FIG. 4) generated by alanine scanning mutagenesis. Antibody substitution of the first 10 amino acids of the 12 amino acid extracellular region of CD52 was conducted on human CD52 cDNA in pcDNA3.1 expression vector (Invitrogen) using the STRATAGENE QUIKCHANGE II XL site-directed mutagenesis kit. pcDNA3.1 vector encoding wild type or mutant CD52 sequence was sequence-verified and transfected into CHO cells using Lipofectamine™ and by selecting in media containing G418 to generate CHO cell lines that expressed wild type or alanine mutant CD52. Epitope specific binding of anti-human CD52 chimeric antibodies was determined by measuring the binding of the antibodies against the wild type and mutant CD52 expressing cells by FACS. FACS analysis was carried out by detecting the binding of chimeric anti-CD52 antibodies using PE-conjugated goat anti-human secondary antibody (Jackson ImmunoResearch Labs). FIGS. 5A-5C show the Mean Fluorescence Intensity (MFI) of anti-CD52 monoclonal antibodies to wild type and mutant CD52 expressing cell lines. Even though CD52 is a very short, 12 amino acid, GPI anchored protein, the FACS results clearly define that there are three sets of antibodies: (1) N-terminal binding group (such as 4B10); (2) middle binding group (such as 4G7, 9D9 and 11C1) and (3) C-terminal binding group (such as 23E6, 12G6, and 2C3). The epitope specificities of the anti-human CD52 monoclonal antibodies (identified by the abbreviated names described at the end of Example 2) are summarized in Table 8.

TABLE 8 Characteristics of 11 Mouse Anti- Human CD52 Monoclonal Antibodies Epitope Clone Isotype Specificity Rat YTH34.5HL IgG2a 9-10-11-12 Mouse CF1D12 IgG3 3-4-5-6-7 8G3.25.3.5 IgG3 Not confirmed 4G7.F3 IgG3 3-4-5-6-7 9D9.A2 IgG3 3-4-5-6-7 11C11.C5 IgG3 1-3-4-5-6-7 3G7.E9 IgG2b 1-3-4-5-6-7 5F7.1.1.4 IgG3 1-3-4-5-6-7-10 12G6.15.1.2 IgG3 7-8-9 23E6.2.2.1 IgG3 7-8-9 2C3.3.8.1 IgG3 7-8-9-10 7F11.1.9.7 IgG1 1-2-3-4-5 4B10.1.2.4 IgG2a 1-2-3-4-5

CD52 is an extremely small antigen but possesses a relatively large, hydrophilic N-linked glycan moiety as well as a hydrophobic GPI-anchor. To explore the possibility that the sugars might constitute all or part of an epitope recognized by the anti-CD52 antibodies, samples of affinity purified CD52 from CHO-CD52 cells were treated with the endoglycosidase, PNGase-F, to completely remove N-linked sugars from the antigen. Treated and mock-treated control samples were then resolved by SDS-PAGE, blotted to polyvinylidene fluoride (PVDF) membrane (Invitrogen), probed with 3 μg/ml final of each of the anti-CD52 chimeric monoclonal antibodies indicated, and subsequently developed according to standard western blotting procedures using enhanced chemiluminescent detection. Blots with Campath-1H® (C1H) and with secondary antibody alone (2° Alone) were run as positive and negative controls, respectively, and probed with each of the monoclonal antibodies (FIG. 5D). The results revealed different binding preferences amongst the antibodies for glycosylated versus de-glycosylated CD52. This characterization allowed for the categorization of the eleven antibodies into four types of binding groups:

-   -   1. Antibodies exhibiting binding with no apparent preference for         glycosylated versus de-glycosylated CD52 (4G7, 9D9)     -   2. Antibodies exhibiting binding specific for glycosylated CD52         (7F11, 4B10)     -   3. Antibodies exhibiting binding specific for de-glycosylated         CD52 (8G3)     -   4. Antibodies exhibiting binding preferential for         de-glycosylated over glycosylated CD52 (12G6, 5F7, 23E6, 2C3,         11C11, 3G7)

Example 5: CDC Activity of Chimeric Anti-CD52 Antibodies

A complement-dependent cytotoxicity (CDC) assay was performed as described μbelow. Briefly, CHO K1 cells engineered to express CD52 protein (CHO-CD52) were used as target cells and labeled with Na₂ ⁵¹CrO₄ (New England Nuclear, Boston, Mass.) at 37° C. for 1-2 hrs. The cells were washed, resuspended with X-Vivo media, and mixed with anti-human CD52 antibodies to final concentration of 2.2 μg/ml. Human complement (Sigma) was added to the experimental wells to a final concentration of 10%. After a 1-5-hour incubation, 25 μl of cell-free supernatant was collected from each well and counted in a MICROBETA TRILUX Scintillation Counter (Wallac, Gaithersburg, Md.). The amount of ⁵¹Cr spontaneously released was obtained by incubating target cells in medium alone. Spontaneous release from target cells was typically less than 20%. The total amount of ⁵¹Cr incorporated was determined by adding 1% Triton X-100 in distilled water, and the percentage lysis was calculated as follows: [(sample counts per minute (c.p.m.)−spontaneous c.p.m.)/(total c.p.m.−spontaneous c.p.m.)]×100.

Twelve different chimeric anti-CD52 antibodies (mouse variable region and human IgG1 constant region) were tested in CDC assay with human complement on CHO-CD52 cells. Campath-1H® humanized antibody was used as a positive control. A negative control was Campath-1H® null (a non-cell-binding minimal mutant of Campath-1H®—two point mutations in H2 loop-heavy chain CDR2 region (K52bD and K53D; Gilliland L K et al., Journal of Immunology, 162:3663-3671 (1999)). The results indicate that the chimeric antibodies are capable of mediating CDC killing on CD52-expressing cells. Some of the chimeric antibodies mediated robust killing equivalent or better than Campath® (FIG. 6).

Example 6: ADCC Activity of Chimeric Anti-CD52 Antibodies

An antibody-dependent cytotoxicity (ADCC) assay was performed as described below. Briefly, CHO K1 cells engineered to express CD52 protein (CHO-CD52) were used as target cells and labeled with Na₂ ⁵¹CrO₄ (New England Nuclear, Boston, Mass.) at 37° C. for 1-2 hrs. The cells were washed, resuspended with X-Vivo media, and mixed with anti-human CD52 antibodies to final concentration of 1.1 μg/ml. Human PBMC were used as effectors cells and were added at a 1:100 target-to-effector cell ratio. After a 6 hr-overnight incubation, 25 μl of cell-free supernatant was collected from each well and counted in a MICROBETA TRILUX Scintillation Counter (Wallac, Gaithersburg, Md.). The amount of ⁵¹Cr spontaneously released was obtained by incubating target cells in medium alone. Spontaneous release from target cells was typically less than 20%. The total amount of ⁵¹Cr incorporated was determined by adding 1% Triton X-100 in distilled water, and the percentage lysis was calculated as follows: [(sample c.p.m.-spontaneous c.p.m.)/(total c.p.m.−spontaneous c.p.m.)]×100.

Twelve different chimeric anti-CD52 antibodies (mouse variable region and human IgG1 constant region) were tested in ADCC assay using human PBMC as effector cells. Campath-1H® humanized antibody was used as a positive control. Used as a negative control was Campath-1H® null (a non-cell-binding minimal mutant of Campath-1H®—two point mutations in H2 loop-heavy chain CDR2 region (K52bD and K53D; Gilliland, 1999, supra). The results indicate that the chimeric antibodies are capable of mediating ADCC killing on CD52-expressing cells. Some of the chimeric antibodies mediated robust killing equivalent or better than Campath-1H® (FIG. 7).

Example 7: Evaluation of the Binding of Chimeric Anti-CD52 Antibodies to Defined Lymphocyte Population

The following fluorochrome conjugated antibodies were used for flow cytometric analysis: anti-CD3-FITC, anti-CD27-PE, anti-CD62L-PE Cy5, anti-CD56-PE Cy7, anti-CD16-APC Cy7 (BD Biosciences, San Diego, Calif.), anti-CD45RA-ECD (Beckman Coulter), anti-CD19-Pacific Blue, anti-CD4-APC Cy5.5 and anti-CD8 pacific orange (Invitrogen, CA). All the mouse chimeric anti-human CD52 antibodies as well as the humanized Campath-1H® were conjugated to Alexa fluor 647 (BD Pharmingen). Healthy human peripheral blood mononuclear cells were obtained either from cryopreserved buffy coats or from mononuclear cells separated from blood of normal donors obtained from commercial vendors (Bioreclamation, NY, USA). For enrichment of mononuclear cells, human peripheral blood was diluted 1:1 with sterile phosphate buffered saline (PBS) and carefully layered over Ficoll-hypaque (GE Healthcare Bio-Sciences, Uppsala, Sweden) and centrifuged for 30 min at room temperature. The interphase layer of mononuclear cells was drawn out and washed in PBS containing 5% fetal bovine serum (FACS buffer). Contaminating red blood cells (RBCs) were lysed with RBC lysing solution (Sigma, St. Louis, Mo., USA). Cells were resuspended in cold FACS buffer and the debris was removed using a 40 micron filter. Ten color flow cytometry was performed to evaluate the binding ability of 9 chimeric anti-human CD52 antibodies (4B10, 7F11, 9D9, 5F7, 2C3, 4G7, 23E6, 8G3, 3G7) as compared to Campath-1H®.

Briefly, replicates of 1×10⁶ PBMC's in FACS buffer were incubated with a cocktail of pre-titrated dilutions of antibodies against CD3, CD27, CD45RA, CD62L, CD56, CD19, CD8, CD4, CD16 along with one of 9 chimeric anti-human CD52 antibodies (4B10, 7F11, 9D9, 5F7, 2C3, 4G7, 23E6, 8G3, 3G7) for 30 min at 4° C. Cells were washed and fixed in PBS containing 1% paraformaldehyde. 100,000 events of the stained cells were acquired on BD LSR-II (BD Biosciences, San Jose, Calif.) and the data was analyzed using FlowJo 7.2 version Software (Tree Star, Inc, Oregan, USA). Multiple subsets with distinct phenotypic characteristics have been defined among B and T lymphocytes and CD52 has been shown to be expressed on all human lymphocytes. Ten color flow cytometry analysis was performed to identify the lymphocyte subsets, and to assess similarities and the differences in the binding characteristics of anti-CD52 antibodies to cell surface CD52 on defined subsets. Using a combination of markers, 11 phenotypically distinct cell populations corresponding to B, T and NK cell lineages were first defined from the lymphocyte gate. The intensity of staining which corresponds to the ability of anti-CD52 antibodies to detect CD52 expression was then assessed. The histograms (FIGS. 8A-8C) show a comparison of the level of detection of CD52 with each antibody on individual lymphocyte populations. The data shows that the antibodies exhibit significant differences in binding to CD52. The level of detection with 4B10, 9D9, 7F11 and Campath-1H® are comparable, although 4B10 consistently shows the highest level of detection than other antibodies including Campath-1H®, on almost all the cell subsets examined. On the other hand, the detection level of CD52 with 3G7, 4G7, 8G3 and 23E6 antibodies is significantly lower. The results indicate a hierarchy within the antibodies with respect to their ability to recognize CD52 on different cell populations with 4B10 being highest and 3G7 being the lowest. Interestingly, these differences are less obvious on CD4 effector and more so on NK cell subsets on which CD52 appears to be expressed at relatively lower levels. The variations in the binding characteristics indicate that the properties of the chimeric antibodies not only differ significantly from Campath-1H® but also reflect differences in properties among the antibodies.

Example 8: Analysis of Chimeric Anti-CD52 Antibodies in Human CD52 Transgenic Mice (7F11, 8G3, 23E6, 12G6, 4B10 and 5F7)

Human CD52 transgenic mice were administered either Campath® or chimeric anti-CD52 antibodies (7F11, 8G3, 23E6, 12G6, 4B10 and 5F7) to examine the level of lymphocyte depletion. Mice were injected intra-peritoneally with either Campath® or the chimeric anti-CD52 antibodies in a 100 μl volume at a dose of 1 mg/kg. Three days later mice were sacrificed and blood and spleens were collected to determine the level of B and T-cell depletion. Flow cytometry was utilized to evaluate the absolute numbers of total T helper cells, cytotoxic T cells, and B cells present in the circulating peripheral blood or spleens of huCD52 transgenic mice. These lymphocyte populations were defined by their surface expression of the following protein antigens: CD4 expression identifies the T helper cell population, CD8 expression identifies the cytotoxic T cell population and CD19 expression identifies all mature B cell populations. A significant level of T and B-cell depletion was observed for both the 12G6 and 4B10 antibodies, which was comparable to the depletion observed with Campath®. Treatment with either Campath®, the chimeric 12G6 or the chimeric 4B10 antibody significantly reduced T and B cells in both the blood and spleens of treated mice at this dose level. The 7F11 and 5F7 chimeric antibodies resulted in significant levels of T cell depletion level in the blood and spleen but were less effective at depleting B cells in both compartments. Treatment with the 23E6 antibody resulted in a moderate level of depletion at this dose while little to no depletion was observed with the lower affinity 8G3 antibody.

FIGS. 9A-9C show the level of CD4 T cells, CD8 T cells and CD19 B cells in the blood 72 hours after dosing with the chimeric antibodies. FIGS. 10A-10C show the level of CD4 T cells, CD8 T cells and CD19 B cells in the spleen 72 hours after dosing.

Example 9: Analysis of Chimeric Anti-CD52 Antibodies in Human CD52 Transgenic Mice (2C3, 3G7, 4B10, 9D9, and 11C11)

Human CD52 transgenic mice were administered either Campath® or chimeric anti-CD52 antibodies (2C3, 3G7, 4B10, 9D9 and 11C11) to examine the level of lymphocyte depletion. Mice were injected intravenously with either Campath® or the chimeric anti-CD52 antibodies in a 100 μl volume at a dose of 1 mg/kg. Three days later mice were sacrificed and blood and spleens were collected to determine the level of B and T-cell depletion. Flow cytometry was utilized to evaluate the absolute numbers of total T helper cells, cytotoxic T cells, and B cells present in the circulating peripheral blood of huCD52 transgenic mice. These lymphocyte populations were defined by their surface expression of the following protein antigens: CD4 expression identifies the T helper cell population, CD8 expression identifies the cytotoxic T cell population and CD19 expression identifies all mature B cell populations. A significant level of T and B cell depletion was observed for several antibodies in both the blood and spleen. The depleting activity for 2C3 and 9D9 was comparable to that observed with Campath® with significant levels of CD4 and CD8 T cells and CD19 B cells being depleted. Treatment with chimeric 4B10 also resulted in a significant decrease in the numbers of lymphocytes in the blood of transgenic mice. While treatment with either the chimeric antibody 3G7 or 11C11 antibody significantly depleted T cells in the blood, the level of B cells present were not significantly affected at this dose.

FIGS. 11A-11C show the level of CD4 T cells, CD8 T cells and CD19 B cells in the blood 72 hours after dosing with the chimeric antibodies.

Example 10: Analysis of the Efficacy of Anti-CD52 Antibodies (7F11, 4B10 and 12G6)

Forty SCID mice (n=8 per group) were injected with 1×10⁶ B104 tumor cells in 100 μl volume on the right flank. On day 11 post tumor cell injection, treatment began with Campath®, 7F11, 4B10 or 12G6 chimeric antibodies. Antibodies were administered once weekly at 10 mg/kg by intraperitoneal injection throughout the remainder of the experiment. All mice in the untreated group developed progressively growing tumors requiring sacrifice with a median survival of 29 days. Treatment with Campath® resulted in a statistically significant increase in survival compared to the untreated group (median survival (MS) of 50 days and p<0.0001). Treatment with the chimeric anti-CD52 antibodies also resulted in a statistically significant increase in survival compared to untreated mice (p<0.0001 for 7F11 and 4B10 and p=0.0020 for 12G6). Based on survival rates, the activity of both 7F11 and 4B10 antibodies appears to be greater than Campath® (63% survival for 7F11 and 75% survival for 4B10 compared to 50% survival for Campath®). FIG. 12 shows the percent survival of the mice after treatment.

Example 11: Analysis of the Efficacy of Anti-CD52 Antibodies (2C3, 8G3 and 23E6)

Forty SCID mice (n=8 per group) were injected with 1×10⁶ B104 tumor cells in a 100 μl volume on the right flank. On day 11 post tumor cell injection, treatment began with either Campath®, 2C3, 8G3 or 23E6 chimeric antibodies. Antibodies were administered once weekly at 10 mg/kg by intraperitoneal injection throughout the remainder of the experiment. All mice in the untreated group developed progressively growing tumors requiring sacrifice with a median survival of 26 days. Treatment with Campath®, 23E6, and the 2C3 antibody resulted in statistically significant increases in survival (p=0.0025, p=0.0007, and p=0.0002 respectively). FIG. 13 shows the percent survival of the mice after treatment.

Example 12: Analysis of the Efficacy of Chimeric Anti-CD52 Antibodies in a Xenograft Tumor Model (9D9 and 4B10)

Forty SCID mice (n=8 per group) were injected with 1×10⁶ B104 tumor cells in a 100 μl volume on the right flank. On day 11 post tumor cell injection, treatment began with either Campath®, 9D9 or 4B10 chimeric antibody. Antibodies were administered once weekly at 10 mg/kg by intraperitoneal injection throughout the remainder of the experiment. All mice in the untreated group developed progressively growing tumors requiring sacrifice with a median survival of 27 days. Treatment with Campath® resulted in a statistically significant increase in survival compared to the untreated group (median survival not achieved and p<0.0001). Treatment with the chimeric anti-CD52 antibodies also resulted in a statistically significant increase in survival compared to untreated mice (p<0.0001 for 9D9 and 4B10). Statistical analysis of the survival curves reveals that the 9D9 chimeric antibody displayed activity comparable to Campath® (p=0.0675) in this experiment. FIG. 14 shows the percent survival of the mice after treatment.

Example 13: Analysis of the Efficacy of Chimeric Anti-CD52 Antibodies in a Xenograft Tumor Model (2C3 and 11C11)

Forty SCID mice (n=8 per group) were injected with 1×10⁶ B104 tumor cells in a 100 μl volume on the right flank. On day 11 post tumor cell injection, treatment began with either Campath®, 2C3 or 11C11 chimeric antibody. Antibodies were administered once weekly at 10 mg/kg by intraperitoneal injection throughout the remainder of the experiment. All mice in the untreated group developed progressively growing tumors requiring sacrifice with a median survival of 32 days. Treatment with Campath® resulted in a statistically significant increase in survival compared to the untreated group (median survival not achieved and p<0.0001). Treatment with the chimeric anti-CD52 antibodies also resulted in a statistically significant increase in survival compared to untreated mice (p<0.0001 for 2C3 and p=0.0004 for 11C11). Statistical analysis of the survival curves reveals that both the 2C3 and 11C11 chimeric antibodies displayed activity comparable to Campath® (p=0.3173 for 2C3 and p=0.9703 for 11C11). FIG. 15 shows the percent survival of the mice after treatment with Campath®, 2C3 chimeric antibody or 11C11 chimeric antibody.

Example 14: Generation and Analysis of Humanized Anti-CD52 Antibody 4B10

Humanized anti-human CD52 antibody 4B10 was generated by grafting the CDR regions from the mouse 4B10 antibody into a human antibody variable region framework. Mouse 4B10 heavy chain and light chain sequences were evaluated by a web-based sequence alignment in order to identify a human germline heavy chain and light chain framework sequence that would serve as a suitable acceptor for the CDR graft (FIG. 16). The residues defining the CDR regions by Kabat and IMGT® were superimposed into human framework regions that have high sequence identity to generate humanized heavy chain and light chain sequences. Visual inspection and sequence analysis of the superimposed 4B10 heavy and light chain sequences was carried out to identify the most suitable acceptor sequence. Of all the germline sequences that have high similarity, the VH3-72 germline sequence for heavy chain and the VK2-A18b for light chain (human germ line sequences can be found at the website described in the publication by Tomlinson, I M, et al., EMBO J., 14(18):4628-4638 (1995); Cook, G P., et al., Nature Genetics, 7:162-168 (1994)) were selected from their high degree of homology, sequence similarity to mouse framework regions and for minimal disruption of CDR loop structure as CDR acceptor sequence. CDR1, 2, and 3 sequences of heavy chain and light chain for 4B10 were grafted into VH3-72 and VK2-A18b human framework regions respectively to generate humanized heavy chain and light chain sequences for 4B10 (illustrated in FIG. 17; FIG. 110).

Example 15: Assessment of the Binding Activities of Chimeric and Humanized 4B10 Monoclonal Antibodies

Chimeric and humanized 4B10 antibodies were produced and purified as described in Example 3 and analyzed for their ability to bind to the B cell line B104, which endogenously expresses CD52, by FACS. Briefly, 2×10⁵ B104 cells were incubated with antibody (0.02 μg/ml to 16.7 μg/ml) in PBS containing 5% fetal bovine serum and 5% goat serum. The bound antibody was detected with FITC labeled goat anti-human secondary antibody which detected chimeric or humanized anti-CD52 antibodies. Labeled cells were analyzed using a FACSCalibur system (Becton Dickinson). FIG. 18 shows the fold increase in Geometric mean fluorescence intensity of each sample normalized (divided) to that of 2°-only sample. The 11 different concentrations (12^(th) point on X axis is secondary alone) of the humanized and chimeric antibody used in the assay is shown on the X axis and the Geo Mean fold increase in the mean fluorescence is on the Y axis. The results indicate that the humanized 4B10 antibody bound as well or slightly better than chimeric 4B10 antibody to CD52 expressing cells.

Example 16: Assessment of the ADCC Activities of Chimeric and Humanized 4B10 Monoclonal Antibodies

Humanized and chimeric 4B10 antibodies were evaluated for their ability to mediate ADCC killing of CD52-expressing cells. An ADCC assay was carried out as described above in Example 6. Briefly, CHO K1 cells engineered to express CD52 protein (CHO-CD52) were used as target cells and labeled with Na₂ ⁵¹CrO₄ (New England Nuclear, Boston, Mass.) at 37° C. for 1-2 hrs. The cells were washed, resuspended in RPMI 1640 media with 10% FCS, and mixed with chimeric or humanized 4B10 antibodies at various concentrations ranging from 10 μg/ml to 0.01 μg/ml. Human PBMC were used as effectors cells and were added at 1:50 target-to-effector cell ratio. After a 6 hr-overnight incubation, 25 μl of cell-free supernatant was collected from each well and counted in a MICROBETA TRILUX Scintillation Counter (Wallac, Gaithersburg, Md.). The amount of ⁵¹Cr spontaneously released was obtained by incubating target cells in medium alone. Spontaneous release from target cells was typically less than 20%. The total amount of ⁵¹Cr incorporated was determined by adding 1% Triton X-100 in distilled water, and the percentage lysis was calculated as follows: [(sample c.p.m.-spontaneous c.p.m.)/(total c.p.m.-spontaneous c.p.m.)]×100.

FIG. 19 illustrates the concentrations of control, chimeric and humanized 4B10 antibodies used in the assay (X axis) and the Y axis shows % specific killing. The results indicate that humanized 4B10 antibody mediated equivalent or slightly better ADCC killing than chimeric 4B10 antibody. The control IgG1 isotype control showed only low levels of background killing at the concentrations tested.

Example 17: Assessment of the CDC Activities of Chimeric and Humanized 4B10 Monoclonal Antibodies

Humanized and chimeric 4B10 antibodies were evaluated for their ability to mediate cytotoxic effect on B104 cells that endogenously express CD52 in the presence of human complement. CellTiter Glo kit (Promega) was used to determine the live cells remaining in the assay. Briefly, B104 cells (target cells) were plated at 2.5×10⁴ cells/well in a 96 well plate and were mixed with chimeric or humanized 4B10 antibody at various concentrations ranging from 1 μg/ml to 25 μg/ml and human complement to a final concentration of 10%. Complement alone without the antibody and antibody alone without complement were used as controls to determine the background. After three hours of incubation at 37° C., plates were centrifuged for 3 min at 1500 rpm and the live cells present in the pellet were determined using CellTiter Glo assay. Plates were read on Envision machine. FIG. 20 shows the live cells present in the assay as measured using CellTiter Glo assay. Again, with the increasing concentrations of the humanized and chimeric 4B10 antibody there is a decrease in the number of live cells. These results suggest that the humanized antibody performed as well as or slightly better than chimeric 4B10 antibody in CDC mediated killing of B104 cells.

Example 18: Analysis of Pharmacokinetic Profile of Chimeric and Humanized Anti-CD52 Antibodies in CD52 Transgenic Mice (12G6, 7F11, Chimeric and Humanized 4B10)

Human CD52 transgenic mice were administered one of Campath®, 12G6, 7F11, and chimeric and humanized 4B10 anti-CD52 antibodies to examine the level of lymphocyte depletion. Mice were injected intravenously with one of those antibodies in a 100 μl volume at a dose of 1 mg/kg. For analysis of anti-antibody responses, 100 μl of blood was collected into serum separator tubes via puncture of the retro-orbital plexus at 2 hours, 1, 2, 4, 7, and 10 days post antibody injection. ELISA analysis was used to determine the level of circulating human IgG1 in each serum sample. Based on circulating levels of antibody, there appears to be little to no difference between Campath®, 7F11, and the chimeric and humanized forms of 4B10. The 12G6 antibody displayed lower cmax values following injection, suggesting that this antibody may be degraded more quickly. FIG. 21 shows the pharmacokinetic profile of Campath®, 12G6 (chimeric), 7F11 (chimeric), 4B10 (chimeric) and 4B10 (humanized) antibodies.

Example 19: Analysis of the Depleting Activity of Chimeric and Humanized Anti-CD52 Antibodies in CD52 Transgenic Mice (Chimeric and Humanized 4B10)

Human CD52 transgenic mice were administered either Campath® or chimeric or humanized 4B10 anti-human CD52 antibody to examine the level of lymphocyte depletion. Mice were injected intravenously with either Campath® or the chimeric or humanized 4B10 anti-human CD52 antibody in a 100 μl volume at a dose of 0.1 mg/kg. Three days later mice were sacrificed and blood and spleens were collected to determine the level of B and T-cell depletion. Flow cytometry was utilized to evaluate the absolute numbers of total T helper cells, cytotoxic T cells, and B cells present in the circulating peripheral blood of the huCD52 transgenic mice. These lymphocyte populations were defined by their surface expression of the following protein antigens: CD4 expression identifies the T helper cell population, CD8 expression identifies the cytotoxic T cell population and CD19 expression identifies all mature B cell populations. Comparison of the depleting activity in the spleen revealed that there was no difference in the level of T cells depleted following administration of either Campath® or the chimeric or humanized forms of 4B10. Due to the low dose used, only a modest level of depletion of B cells was observed in the spleen. On a per animal basis it appears that the humanized 4B10 antibody is as good or slightly better than Campath® at mediating lymphocyte depletion. FIGS. 22A-22C show the level of CD4 T cells, CD8 T cells and CD19 B cells in the blood 72 hours after dosing with the chimeric and humanized antibodies.

Example 20: Relative Binding Efficiency of Anti-Human CD52 Antibodies

The EC₅₀ values of selected anti-CD52 antibodies were estimated using CHO cells engineered to express CD52. CHO-CD52 cells were trypsinized in 0.25% trypsin, collected, and rinsed with PBS/5% FBS. Cells were then deposited into round-bottom 96 well plates at 1E5 cells per well. Primary antibody staining was done with a 12 point serial dilution (1:2) of each anti-CD52 chimeric antibody starting at 50 μg/mL. FITC-conjugated goat FAB2 fragment of anti-human Fc gamma at 10 μg/mL (Jackson 109-096-098) secondary was used. Cells were washed 3 times in ice-cold PBS/5% FBS before and after each incubation. Cells were fixed with PBS containing 2% methanol-free paraformaldehyde and evaluated by flow cytometry. The flow cytometry data was analyzed using Graph pad Prizm software to determine EC₅₀ value with 95% confidence interval.

Binding data (FIG. 23) indicates that the new CD52 antibodies not only have different epitope specificities as mentioned earlier, but also have different binding characteristics as shown in the table given below. Campath-1H®, 7F11, 4B10, 2C3 and 12G6 chimeric antibodies showed relatively similar EC 50 values between 0.5 to 2.5 μg/ml/. 9D9 chimeric antibody showed slightly different binding characteristics with EC₅₀ value around 5 to 7 μg/ml. 4B10 humanized antibody showed similar binding characteristics as that of chimeric 4B10 antibody, indicating that the humanized antibody retained the binding characteristics as that of chimeric 4B10 antibody.

TABLE 9 EC50 (μg/mL) Clone ID Mean STDEV C1H* 1.36 0.46 2C3-Chi 1.32 0.33 4B10-Chi 2.18 0.33 4B10-H1/K1 2.23 0.50 7F11-Chi 2.22 0.29 9D9-Chi 6.05 1.18 12G6-Chi 0.95 0.21 *C1H refers to Campath-1H ®.

Example 21: Humanization of Anti-CD52 Antibody Clone 7F11

Humanization of anti-human CD52 antibody clone 7F11 was performed by grafting the CDR regions from the mouse 7F11 antibody into a human antibody variable region framework as described in Example 14 for 4B10 antibody humanization. CDR-1, CDR-2, and CDR-3 sequences of the heavy chain and light chain of 7F11 were grafted into VH3-72 and VK2 A18b human framework regions, respectively. The human JH6 (WGQGTTVTVSS: SEQ ID NO: 133) and JK2 (FGQGTKLEIK: SEQ ID NO: 134) sequences were selected as the C-terminal peptides for the humanized heavy and light chains, respectively, to generate humanized heavy chain (7F11-SFD1 and 7F11-SFD2) and humanized light chain (7F11-VK2) variable region sequences for 7F11 (FIG. 24). The two humanized heavy chain variable region sequences (7F11-SFD1 and 7F11-SFD2) differ by one amino acid residue in the CDR-3 region. The 7F11-SFD1 version has a threonine at position 93 (denoted by the Kabat numbering system), while the 7F11-SFD2 version has an alanine at this position. Position 93 is underlined for both 7F11-SFD1 and 7F11-SFD2 in FIG. 24.

The full-length heavy chain amino acid sequence of 7F11-SFD1 (SEQ ID NO: 274) and the full-length light chain amino acid sequence of 7F11-K2 (SEQ ID NO: 275) are shown in FIG. 107.

Example 22: Assessment of the Binding Activities of Chimeric and Humanized 7F11 Monoclonal Antibodies

Chimeric and humanized 7F11 antibodies (7F11-SFD1/K2 and 7F11-SFD2/K2) were produced and purified using the methods described in Example 3, and analyzed for their ability to bind to CD52 expressed on the surface of CHO-CD52 cells (CHO cells engineered to express human CD52) by flow cytometry. Briefly, 2×10⁵ CHO-CD52 cells were incubated with an antibody at 10 μg/ml in PBS containing 5% fetal bovine serum and 5% goat serum. Bound antibody was detected with a FITC-labeled goat anti-human secondary antibody which detected chimeric or humanized anti-CD52 antibodies. Labeled cells were analyzed using a FACSCalibur system (Becton Dickinson) and the data was analyzed using FlowJo version 7.2 software (Tree Star, Inc, Oregon, USA). The histogram in FIG. 25 compares the levels of CD52 detected with chimeric and humanized 7F11 antibodies. The results indicate that the humanized 7F11 antibodies bound as well or slightly better than the chimeric 7F11 antibody to CD52 expressing cells.

Example 23: Humanization of Anti-CD52 Antibody Clone 2C3

Humanization of anti-human CD52 antibody clone 2C3 was performed by grafting the CDR regions from the mouse 2C3 antibody into a human antibody variable region framework as described in Example 14 for clone 4B10 antibody humanization. CDR-1, CDR-2, and CDR-3 sequences of the heavy chain and light chain of 2C3 were grafted into VH3-72 and VK2 A18b human framework regions, respectively. The human JH6 (WGQGTTVTVSS: SEQ ID NO: 133) and JK5 (FGQGTRLEIK: SEQ ID NO: 135) sequences were selected as the C-terminal peptides for the humanized heavy and light chains, respectively, to generate humanized heavy chain (2C3-SFD1) and light chain (2C3-VK1) variable region sequences for 2C3 (FIGS. 26A and B). Unlike humanized clones 4B10 and 7F11, the binding affinity for the CDR-grafted humanized 2C3 antibody was greatly reduced. Binding affinity was restored by introducing back mutations to the CDR-grafted structure, with the aim of limiting the number of back mutations to a minimum to keep the reshaped antibody as “human” as possible, thus reducing the possibility of immunogenicity. Single or multiple back mutations were incorporated into both the humanized heavy and light chain variable region sequences. The positions of the back mutations (as denoted by the Kabat numbering system) are depicted in Table 10 and Table 11 below. Antibodies generated with these back mutations were evaluated for restored binding affinity. Three light chain variants (2C3-VK1(L46R), also referred to as 2C3-VK11; 2C3-VK1(Y36L-L46R), also referred to as 2C3-VK12; and 2C3-VK1(M4I-A19V-Y36L-Q45K-L46R), also referred to as 2C3-VK13) and 5 heavy chain variants (2C3-SFD1(L78V), also referred to as 2C3-VH12; 2C3-SFD1(G49A), also referred to as 2C3-VH15; 2C3-SFD1(G49A-L78V), also referred to as 2C3-VH16; 2C3-SFD1(L18M-G49A-L78V), also referred to as 2C3-VH17; and 2C3-SFD1(L18M-G42E-G49A-L78V), also referred to as 2C3-VH19) were generated using standard molecular biology techniques. The amino acid sequences for CDR-grafted heavy chain variable region sequence 2C3-SFD1 and back mutants 2C3-VH12, 2C3-VH15, 2C3-VH16, 2C3-VH17, and 2C3-VH19 are shown in FIG. 26A with the back mutated amino acids underlined and the CDRs boldfaced. Similarly, for the light chain sequences, CDR-grafted variable region sequence 2C3-VK1 and back mutants 2C3-VK11, 2C3-VK12, and 2C3-VK13 are shown in FIG. 26B with the back mutated amino acids underlined and the CDRs boldfaced.

The full-length heavy chain amino acid sequence of 2C3-SFD1 (SEQ ID NO: 272) and the full-length light chain amino acid sequence of 2C3-K12 (SEQ ID NO: 273) are shown in FIG. 106.

TABLE 10 2C3 clone heavy chain back mutants Clone ID Mutation (Kabat numbering position) 2C3-VH12 L to V (78) 2C3-VH15 G to A (49) 2C3-VH16 G to A (49), L to V (78) 2C3-VH17 L to M (18), G to A (49), L to V (78) 2C3-VH19 L to M (18), G to E (42), G to A (49), L to V (78)

TABLE 11 2C3 clone light (kappa) chain back mutants Clone ID Mutation (Kabat numbering position) 2C3-VK11 L to R (46) 2C3-VK12 Y to L (36) and L to R (46) 2C3-VK13 M to I (4), A to V (19), Y to L (36), QL to KR (45, 46)

Example 24: Assessment of the Binding Activities of Chimeric and Humanized 2C3 Monoclonal Antibodies

Chimeric and humanized 2C3 antibodies were produced and purified using the methods described in Example 3. A number of the humanized antibodies produced by pairing heavy chain variants with light chain variants, and a corresponding chimeric antibody, were analyzed by flow cytometry for their ability to bind to CD52 expressed on the surface of CHO-CD52 cells, using the methods described in Example 22. The binding data suggest that clones generated by pairing heavy chain variants with light chain variants 2C3-VK1 or 2C3-VK11 had reduced binding ability, while clones generated by pairing heavy chain variants with 2C3-VK12 or 2C3-VK13 showed binding equivalent to or better than that of a chimeric 2C3 antibody. A representative histogram of selected clones (FIG. 27A) compares the level of CD52 detected by chimeric and humanized 2C3 antibodies. Binding of 2C3-SFD1/K1 is reduced significantly compared to that of the corresponding chimeric antibody. Incorporating a single mouse residue at position 46 (leucine to arginine) in the light chain (resulting in 2C3-VK11) did not restore the binding when paired with heavy chain 2C3-SFD1 to make antibody 2C3-SFD1/K11. Further, binding was not restored by incorporating three back mutations in the heavy chain (resulting in 2C3-VH17) to make antibody 2C3-H17/K11. However, binding was completely restored when the 2C3-SFD1 heavy chain was paired with 2C3-VK12, which has two back mutations, to make antibody 2C3-SFD1/K12, suggesting that specific back mutations need to be incorporated to restore binding avidity. FIG. 27B shows a histogram of selected humanized clones that demonstrate binding equivalent to that of a chimeric 2C3 antibody. These results indicate that the back mutation of two amino acid residues in the 2C3-VK12 light chain was sufficient to completely restore antibody avidity. The changes at residues 36 (Y to L) and 46 (L to R) were able to restore binding when paired with almost any heavy chain variant. As such, the humanized 2C3 clone showing restored binding with minimal framework residues derived from the original mouse antibody is 2C3-SFD1/K12.

Example 25: Humanization of Anti-CD52 Antibody Clone 12G6

Humanization of anti-human CD52 antibody clone 12G6 was performed by grafting the CDR regions from the mouse 12G6 antibody into a human antibody variable region framework as described in Example 14 for clone 4B10 antibody humanization. CDR-1, CDR-2, and CDR-3 sequences of the heavy chain and light chain of 12G6 were grafted into VH3-72 and VK2 A18b human framework regions, respectively. The human JH6 (WGQGTTVTVSS: SEQ ID NO: 133) and JK2 (FGQGTKLEIK: SEQ ID NO: 134) sequences were selected as the C-terminal peptides for the humanized heavy and light chains, respectively, to generate humanized heavy chain (12G6-SFD1) and light chain (12G6-VK1) variable region sequences for 12G6 (FIGS. 28A and 28B). When the 12G6-SFD1 heavy chain variable region and 12G6-VK1 light chain variable region were combined in the humanized 12G6-SFD1/K1 antibody, the binding affinity for CD52 was greatly reduced. Binding affinity was restored by introducing back mutations to the CDR grafted structure. Single or multiple back mutations were incorporated into both the humanized heavy and light chain variable region sequences. The positions of these back mutations (as denoted by the Kabat numbering system) are depicted in Table 12 and Table 13 below. Antibodies generated with these back mutations were evaluated for restored binding affinity. Four light chain variants (12G6-VK1(Y36V), also referred to as 12G6-VK10; 12G6-VK1(Y36V-Q45K-L46R), also referred to as 12G6-VK11; 12G6-VK1(Y36V-L46R), also referred to as 12G6-VK12; and 12G6-VK1(L46R), also referred to as 12G6-VK13) and three heavy chain variants (12G6-SFD1(L78V), also referred to as 12G6-VH10; 12G6-SFD1(G49A), also referred to as 12G6-VH11; and 12G6-SFD1(G49A-L78V), also referred to as 12G6-VH12) were generated using standard molecular biology techniques. The amino acid sequences for the CDR grafted heavy chain variable region sequence 12G6-SFD1 and back mutants 12G6-VH10, 12G6-VH11, and 12G6-VH12 are shown in FIG. 28A with the back mutated amino acids underlined and the CDRs boldfaced. Similarly, for the light chain sequences, CDR grafted variable region sequence 12G6-VK1 and back mutants 12G6-VK10, 12G6-VK11, 12G6-VK12, and 12G6-VK13 are shown in FIG. 28B with the back mutated amino acids underlined and the CDRs boldfaced.

The full-length heavy chain amino acid sequence of 12G6-SFD1 (SEQ ID NO: 279) and the full-length light chain amino acid sequence of 12G6-K12 (SEQ ID NO: 280) are shown in FIG. 109.

TABLE 12 12G6 clone heavy chain back mutants Clone ID Mutation (Kabat numbering position) 12G6-VH10 L to V (78) 12G6-VH11 G to A (49) 12G6-VH12 G to A (49) and L to V (78)

TABLE 13 12G6 clone light (kappa) chain back mutants Clone ID Mutation (Kabat numbering position) 12G6-VK10 Y to V (36) 12G6-VK11 Y to V (36), QL to KR (45, 46) 12G6-VK12 Y to V (36), L to R (46) 12G6-VK13 L to R (46)

Example 26: Assessment of the Binding Activities of Chimeric and Humanized 12G6 Monoclonal Antibodies

Chimeric and humanized 12G6 antibodies were produced and purified using the methods described in Example 3. A number of the humanized antibodies produced by pairing heavy chain variants with light chain variants, and a corresponding chimeric antibody, were analyzed by flow cytometry for their ability to bind to CD52 expressed on the surface of CHO-CD52 cells, using the methods described in Example 22. The binding data suggest that clones generated by pairing heavy chain variants with light chain variants 12G6-VK1, 12G6-VK10, or 12G6-VK13 had reduced binding ability, while clones generated by pairing heavy chain variants with 12G6-VK11 or 12G6-VK12 showed binding equivalent to or better than that of the corresponding chimeric 12G6 antibody. A representative histogram of selected clones (FIG. 29) compares the level of CD52 detected by chimeric and humanized 12G6 antibodies. These results indicate that the back mutation of two amino acid residues in the 12G6 light chain variable region (clone 12G6-VK12) was sufficient to completely restore antibody specificity. The changes at Kabat numbering residues 36 (Y to V) and 46 (L to R) were able to restore binding when paired with almost any heavy chain variant. As such, the humanized 12G6 clone showing restored binding with minimal framework residues derived from the original mouse antibody is 12G6-SFD1/K12.

Example 27: Humanization of Anti-CD52 Antibody Clone 9D9

Humanization of anti-human CD52 antibody clone 9D9 was performed by grafting the CDR regions from the mouse 9D9 antibody into a human antibody variable region framework as described in Example 14 for clone 4B10 antibody humanization. CDR-1, CDR-2, and CDR-3 sequences of the heavy chain and light chain of 9D9 were grafted into VH3-23 and VK2 A18b human framework regions, respectively. The human JH6 (WGQGTTVTVSS: SEQ ID NO: 133) and JK2 (FGQGTKLEIK: SEQ ID NO: 134) sequences were selected as the C-terminal peptides for the humanized heavy and light chains, respectively, to generate humanized heavy chain (9D9-VH10) and light chain (9D9-VK2) variable region sequences (FIGS. 30A and 30B). When the 9D9-VH10 heavy chain and 9D9-VK2 light chain were combined in the humanized 9D9-H10/K2 antibody, the binding affinity for CD52 was greatly reduced. Binding affinity was restored by introducing back mutations to the CDR grafted structure. Single or multiple back mutations were incorporated into both the humanized heavy and light chain variable region sequences. The positions of the back mutations (as denoted by the Kabat numbering system) are depicted in Table 14 and Table 15 below. Antibodies generated with these back mutations were evaluated for restored binding affinity. Four light chain variants (9D9-VK2(Y36L-Q45K-L46R), also referred to as 9D9-VK12; 9D9-VK2(Y36L-L46R), also referred to as 9D9-VK13; 9D9-VK2(L46R), also referred to as 9D9-VK14; and 9D9-VK2(Q45K-L46R), also referred to as 9D9-VK15) and five heavy chain variants (9D9-VH10(W47L-V48T-549A-N765-L78V), also referred to as 9D9-VH11; 9D9-VH10(W47L-V48T-S49A), also referred to as 9D9-VH15; 9D9-VH10(W47L), also referred to as 9D9-VH16; 9D9-VH10(W47L-V48T), also referred to as 9D9-VH17; and 9D9-VH10(W47L-S49A), also referred to as 9D9-VH18) were generated using standard molecular biology techniques. The amino acid sequences for CDR-grafted heavy chain variable region sequence 9D9-VH10 and back mutants 9D9-VH11, 9D9-VH15, 9D9-VH16, 9D9-VH17, and 9D9-VH18 are shown in FIG. 30A with the back mutated amino acids underlined and the CDRs boldfaced. Similarly, for the light chain sequences, CDR-grafted variable region sequence 9D9-VK2 and back mutants 9D9-VK12, 9D9-VK13, 9D9-VK14, and 9D9-VK15 are shown in FIG. 30B with the back mutated amino acids underlined and the CDRs boldfaced.

The full-length heavy chain amino acid sequences of 9D9-H16 (SEQ ID NO: 276) and 9D9-H18 (SEQ ID NO: 277), and the full-length light chain amino acid sequence of 9D9-K13 (SEQ ID NO: 278) are shown in FIG. 108.

TABLE 14 9D9 heavy chain back mutants Clone ID Mutation (Kabat numbering position) 9D9-VH11 WVS to LTA (47-49), N to S (76), L to V (78) 9D9-VH15 WVS to LTA (47-49) 9D9-VH16 W to L (47) 9D9-VH17 WV to LT (47, 48) 9D9-VH18 W to L (47) and S to A (49)

TABLE 15 9D9 light (kappa) chain back mutants Clone ID Mutation (Kabat numbering position) 9D9-VK12 Y to L (36) and QL to KR (45, 46) 9D9-VK13 Y to L (36) and L to R (46) 9D9-VK14 L to R (46) 9D9-VK15 QL to KR (45, 46)

Example 28: Assessment of the Binding Activities of Chimeric and Humanized 9D9 Monoclonal Antibodies

Chimeric and humanized 9D9 antibodies were produced and purified using the methods described in Example 3. A number of the humanized antibodies produced by pairing heavy chain variants with light chain variants, and a corresponding chimeric antibody, were analyzed by flow cytometry for their ability to bind to CD52 expressed on the surface of CHO-CD52 cells (CHO cells engineered to express human CD52), using the methods described in Example 22. The binding data suggest that clones generated by pairing heavy chain variants with light chain variants 9D9-VK2, 9D9-VK14, or 9D9-VK15 had reduced binding ability, while clones generated by pairing 9D9-VK12 or 9D9-VK13 light chain variants with back mutated heavy chain variants 9D9-VH11, 9D9-VH15, 9D9-VH16, and 9D9-VH18 showed binding equivalent to or better than that of the corresponding chimeric 9D9 antibody. When light chain variants 9D9-VK12 and 9D9-VK13 were paired with the parental CDR grafted heavy chain 9D9-VH10 or the back mutated 9D9-VH17 sequence, binding was significantly reduced, suggesting that for humanized 9D9 clones, both heavy chain and light chain sequences have to be engineered with back mutations to restore binding ability. A representative histogram of selected clones (FIG. 31) compares the level of CD52 detected by chimeric and humanized 9D9 antibodies. These results indicate that the back mutation of two amino acid residues (e.g., Y to L at position 36, and L to R at position 46) in the 9D9 light chain variable region (clone 9D9-VK13) was necessary to restore antibody specificity when paired with heavy chains that were mutated at one position (e.g., W to L, at position 47) or at two positions (e.g., W to L at position 47 and S to A at position 49). As such, the humanized 9D9 clones showing restored binding with minimal framework residues derived from the original mouse antibody are 9D9-H16/K13 and 9D9-H18/K13.

Example 29: Determination of Relative Binding Efficiency of Humanized Anti-Human CD52 Antibodies

The EC₅₀ values of chimeric and humanized anti-CD52 antibodies were estimated using CD4+ T cells isolated from healthy donor PBMCs obtained from commercial sources (Bioreclamation, NY, USA). CD4+ T cells were isolated by negative selection using an EasySep kit (Stem Cell Technologies). CD4+ T cells isolated from huCD52 transgenic CD1 mouse spleen tissue were also used (Stem Cell Technologies) according to the methods described above in Example 20 for CHO-CD52 cells. Briefly, human CD4+ T cells were isolated from 50 ml of peripheral blood from healthy volunteers (Bioreclamation), and huCD52 transgenic mouse CD4+ T cells were isolated from spleen tissue. Cells were rinsed with PBS/5% FBS and deposited into round-bottom 96 well plates at 1×10⁵ cells per well. Primary antibody staining was done with an 8 point serial dilution (1:3) of each anti-CD52 chimeric and humanized antibody starting at 100 pg/mL. A FITC-conjugated goat F(ab′)2 fragment of anti-human Fc gamma at 10 pg/mL (Jackson 109-096-098) secondary antibody was used. Cells were washed 3 times in ice-cold PBS/5% FBS before and after each incubation. Cells were fixed with PBS containing 2% methanol-free paraformaldehyde and evaluated by flow cytometry. The flow cytometry data was analyzed using GraphPad Prism software to determine an EC₅₀ value with 95% confidence interval. Based on the binding of anti-CD52 antibodies to CD4+ T cells isolated from human PBMCs and to CD4+ T cells isolated from spleen tissue of human CD52 transgenic mice, binding curves (FIGS. 32A, 32B, 32C) were generated and EC₅₀ values estimated and shown in FIG. 33. All of the antibodies showed similar binding characteristics to both human CD4+ T cells and to CD4+ T cells isolated from human CD52 transgenic mice. Binding data indicate that the humanized antibodies have equivalent or better binding affinities compared to their parental chimeric antibodies, suggesting that binding affinity is retained or improved upon humanization. Humanized 2C3 and 12G6 antibodies have at least two fold lower EC₅₀ values than a Campath-1H® antibody as determined by this cell binding assay.

Example 30: Evaluation of the Binding of Humanized Anti-CD52 Antibodies to a Defined Lymphocyte Population

Campath-1H® (C1H) and humanized 2C3 (2C3-SFD1/K12), 9D9 (9D9-H16/K13 and 9D9-H18/K13), and 12G6 (12G6-SFD1/K11, 12G6-SFD1/K12) antibodies were evaluated for their binding to various PBMC subsets in normal donor PBMCs using the methods described above in Example 7 for chimeric anti-CD52 antibodies. A number of fluorochrome conjugated antibodies were used for flow cytometric analysis. Anti-CD27-PE, anti-CD19 and anti-CD11c-PE Cy5, anti-CD56 and anti-CD123-PE Cy7, anti-CD16-APC Cy7, and CD4-APC were obtained from BD Biosciences (San Diego, Calif.), while anti-CD54RA-ECD and anti-HLA-DR-ECD were obtained from Beckman Coulter. Anti-CD3-Pacific Blue, anti-CD8 and anti-CD14-Pacific Orange, and anti-CD4-APC cy5.5 were obtained from Invitrogen (CA). All of the humanized anti-human CD52 antibodies (9D9-H18/K13, 9D9-H16/K13, 12G6-SFD1/K11, 12G6-SFD1/K12, and 2C3-SFD1/K12) as well as the Campath-1H® were conjugated to FITC. Healthy human peripheral blood mononuclear cells were obtained either from cryopreserved buffy coats or from mononuclear cells separated from the blood of normal donors obtained from commercial vendors (Bioreclamation, NY, USA) as described above in Example 7. For enrichment of mononuclear cells, human peripheral blood was diluted 1:1 with sterile phosphate buffered saline (PBS) and carefully layered over Ficoll-Hypaque (GE Healthcare Bio-Sciences, Uppsala, Sweden) and centrifuged for 30 min at room temperature. The interphase layer of mononuclear cells was drawn out and washed in PBS containing 5% fetal bovine serum (FACS buffer). Contaminating red blood cells (RBCs) were lysed with RBC lysing solution (Sigma, St. Louis, Mo., USA). Cells were resuspended in cold FACS buffer and the debris was removed using a 40 μm filter. Multi color flow cytometry was performed to evaluate the binding ability of humanized anti-human CD52 antibodies 2C3 (2C3-SFD1/K12), 9D9 (9D9-H16/K13 and 9D9-H18/K13) and 12G6 (12G6-SFD1/K11 and 12G6-SFD1/K12) as compared to Campath-1H®.

Briefly, replicates of 1×10⁶ PBMCs in FACS buffer were incubated with cocktails of pre-titrated dilutions of antibodies to examine either lymphocyte or myeloid derived cells. The lymphocyte cocktail comprised antibodies against CD3, CD27, CD45RA, CD56, CD19, CD8, CD4, and CD16. The antibody cocktail to define myeloid populations included antibodies against HLA-DR, CD11 c, CD123, CD4, and CD14. In each of the cocktails, one of the anti-CD52 antibodies was included at 10 μg/ml concentration. The cells were stained for 30 min at 4° C. and were washed and fixed in PBS containing 1% paraformaldehyde. 100,000 events of the stained cells were acquired on a BD LSR II flow cytometer (BD Biosciences, San Jose, Calif.), and the data was analyzed using FlowJo version 7.2 software (Tree Star, Inc, Oregon, USA). Multiple subsets with distinct phenotypic characteristics have been defined among B and T lymphocytes, and CD52 has been shown to be expressed on all human lymphocytes. Multi color flow cytometry analysis was performed to identify the lymphocyte subsets, and to assess similarities and differences in the binding characteristics of the humanized anti-CD52 antibodies to cell surface CD52 on defined subsets. Using a combination of markers, phenotypically distinct cell populations corresponding to B, T, NK and antigen presenting cell lineages were first defined. The intensity of staining, which corresponds to the ability of humanized anti-CD52 antibodies to detect CD52 expression on each of the defined cell populations, was assessed and compared to that of Campath-1H®. The histograms (FIG. 34) compare the level of CD52 detected by each antibody on individual populations. The results indicate that all of the humanized anti-CD52 antibodies bind to cell surface CD52 to a similar extent. Further, no differences were observed between Campath-1H® and humanized anti-CD52 antibodies with respect to the level of detection of cell surface CD52. Analysis was performed on six different donors. Representative data generated using cells derived from one donor is shown in FIG. 34. A similar binding pattern was observed with cells from other donors.

Example 31: Assessment of the ADCC Activities of Chimeric and Humanized 7F11 Monoclonal Antibodies

Humanized and chimeric 7F11 antibodies were evaluated for their ability to mediate ADCC killing of CD52 expressing cells. An ADCC assay was carried out using the methods described above in Example 6. Briefly, CHO K1 cells engineered to express CD52 protein (CHO-CD52) were used as target cells. The target cells were labeled with Na₂ ⁵¹CrO₄ (New England Nuclear, Boston, Mass.) at 37° C. for 2-3 hrs. The cells were washed, re-suspended in RPMI 1640 media with 10% FCS, and mixed with an IgG control antibody, a chimeric 7F11 antibody, or a humanized 7F11 antibody (7F11-SFD1/K2 or 7F11-SFD2/K2) at various concentrations ranging from 5 μg/ml to 0.01 μg/ml. Human NK cells isolated from PBMCs using an NK cell isolation kit (Stem Cell Technologies) were used as effector cells and were added at a 1:5 target to effector cell ratio. After 2-6 hrs incubation, 25 μl of cell-free supernatant were collected from each well and counted in a MicroBeta Trilux Scintillation Counter (Wallac, Gaithersburg, Md.). The amount of ⁵¹Cr spontaneously released was obtained by incubating target cells in medium alone. Spontaneous release from target cells was typically less than 20%. The total amount of ⁵¹Cr incorporated was determined by adding 1% Triton X-100 in distilled water, and the percentage lysis was calculated as follows: [(sample c.p.m.-spontaneous c.p.m.)/(total c.p.m.−spontaneous c.p.m.)]×100. FIG. 35 illustrates the concentrations of control IgG, chimeric 7F11 antibody, and humanized 7F11 antibodies used in the assay (X axis) vs. % specific lysis (Y axis). The results indicate that humanized 7F11 antibodies (7F11-SFD1/K2 and 7F11-SFD2/K2) mediated equivalent or slightly better ADCC killing as compared to a chimeric 7F11 antibody. The control IgG1 isotype showed only low levels of background killing at the concentrations tested.

Example 32: Assessment of the CDC Activities of Chimeric and Humanized 7F11 Monoclonal Antibodies

Humanized and chimeric 7F11 antibodies were evaluated for their ability to mediate complement dependent cytotoxicity (CDC) of CD52 expressing cells. A CDC assay was carried out using the methods described above in Example 5 for chimeric anti-CD52 antibodies. Briefly, CHO K1 cells engineered to express CD52 protein (CHO-CD52) were used as target cells and labeled with Na₂ ⁵¹CrO₄ (New England Nuclear, Boston, Mass.) at 37° C. for 2-3 hrs. The cells were washed, resuspended in RPMI 1640 media, and mixed with an IgG control antibody, a chimeric 7F11 antibody, or a humanized 7F11 antibody (7F11-SFD1/K2 or 7F11-SFD2/K2) at various concentrations ranging from 20 μg/ml to 500 ng/ml. Human complement (Sigma) was added to the experimental wells to a final concentration of 10%. After a 1-5-hour incubation, 25 μl of cell-free supernatant were collected from each well and counted in a MicroBeta Trilux Scintillation Counter (Wallac, Gaithersburg, Md.). The amount of ⁵¹Cr spontaneously released was obtained by incubating target cells in medium alone. Spontaneous release from target cells was typically less than 20%. The total amount of ⁵¹Cr incorporated was determined by adding 1% Triton X-100 in distilled water, and the percentage lysis was calculated as follows: [(sample counts per minute (c.p.m.)−spontaneous c.p.m.)/(total c.p.m.−spontaneous c.p.m.)]×100. FIG. 36 illustrates the concentrations of control IgG, chimeric 7F11 antibody, and humanized 7F11 antibodies (7F11-SFD1/K2 and 7F11-SFD2/K2) used in the assay (X axis) vs. % specific lysis (Y axis). The results indicate that the chimeric 7F11 antibody and humanized antibody 7F11-SFD1/K2 mediated equivalent killing, while humanized antibody 7F11-SFD2/K2 mediated significantly better CDC killing than the chimeric 7F11 antibody. The control IgG1 isotype antibody showed only low levels of background killing at the concentrations tested.

Example 33: Assessment of the ADCC Activities of Chimeric and Humanized 2C3 Monoclonal Antibodies

Humanized and chimeric 2C3 antibodies were evaluated for their ability to mediate ADCC killing of CD52 expressing cells. An ADCC assay was carried out using the methods described above in Example 6, with slight modifications. Briefly, T cells isolated from healthy donor PBMCs using a CD4+ T cell isolation kit (Stem Cell Technologies) were used as target cells. The target cells were labeled overnight with Na₂ ⁵¹CrO₄ (New England Nuclear, Boston, Mass.) at 37° C. The cells were washed, re-suspended in RPMI 1640 media with 10% FCS, and mixed with an IgG control antibody, a chimeric 2C3 antibody, or a humanized 2C3 antibody (2C3-SFD1/K12) at various concentrations ranging from 10 μg/ml to 100 pg/ml. Human NK cells isolated from PBMCs (using an NK cell isolation kit from Stem Cell Technologies) were used as effector cells and were added at a 1:5 target to effector cell ratio. After 2-6 hrs of incubation, 25 μl of cell-free supernatant were collected from each well and counted in a MicroBeta Trilux Scintillation Counter (Wallac, Gaithersburg, Md.). The amount of ⁵¹Cr spontaneously released was obtained by incubating target cells in medium alone. Spontaneous release from target cells was typically less than 20%. The total amount of ⁵¹Cr incorporated was determined by adding 1% Triton X-100 in distilled water, and the percentage lysis was calculated as follows: [(sample c.p.m.-spontaneous c.p.m.)/(total c.p.m.−spontaneous c.p.m.)]×100. FIG. 37 illustrates the concentrations of control IgG, chimeric 2C3 antibody, and humanized 2C3 antibody (2C3-SFD1/K12) used in the assay (X axis) vs. % specific lysis (Y axis). The results indicate that the humanized 2C3 antibody 2C3-SFD1/K12 mediated ADCC killing equivalent to that of the 2C3 chimeric antibody. The IgG1 isotype control showed only low levels of background killing at the concentrations tested.

Example 34: Assessment of the CDC Activities of Chimeric and Humanized 2C3 Monoclonal Antibodies

Humanized and chimeric 2C3 antibodies were evaluated for their ability to mediate complement dependent cytotoxicity (CDC) of CD52 expressing cells. A CDC assay was carried out using the methods described above in Example 5, with slight modifications. Briefly, T cells isolated from healthy donor PBMCs were used as target cells and labeled overnight with Na₂ ⁵¹CrO₄ (New England Nuclear, Boston, Mass.) at 37° C. After overnight labeling, the cells were washed, re-suspended in RPMI 1640 media with 10% FCS, and mixed with an IgG control antibody, a chimeric 2C3 antibody, or a humanized 2C3 antibody (2C3-SFD1/K12) at various concentrations ranging from 10 μg/ml to 10 ng/ml. Human complement (Sigma) was added to the experimental wells to a final concentration of 10%. After a 1-5 hour incubation, 25 μl of cell-free supernatant were collected from each well and counted in a MicroBeta Trilux Scintillation Counter (Wallac, Gaithersburg, Md.). The amount of ⁵¹Cr spontaneously released was obtained by incubating target cells in medium alone. Spontaneous release from target cells was typically less than 20%. The total amount of ⁵¹Cr incorporated was determined by adding 1% Triton X-100 in distilled water, and the percentage lysis was calculated as follows: [(sample counts per minute (c.p.m.)−spontaneous c.p.m.)/(total c.p.m.−spontaneous c.p.m.)]×100. FIG. 38 illustrates the concentrations of control IgG, chimeric 2C3 antibody, and humanized 2C3 antibody (2C3-SFD1/K12) used in the assay (X axis) vs. % specific lysis (Y axis). The results indicate that the chimeric 2C3 antibody and the humanized 2C3 antibody (2C3-SFD1/K12) mediated equivalent lysis. The control IgG1 isotype antibody showed only low levels of background killing at the concentrations tested.

Example 35: Assessment of the ADCC Activities of Chimeric and Humanized 12G6 Monoclonal Antibodies

Humanized and chimeric 12G6 antibodies were evaluated for their ability to mediate ADCC killing of CD52 expressing cells. An ADCC assay was carried out by chromium release assays using T cells isolated from healthy donor PBMCs as target cells, as described above in Example 31. FIG. 39 illustrates the concentrations of control IgG, chimeric 12G6 antibody, and humanized 12G6 antibodies (12G6-SFD1/K11 or 12G6-SFD1/K12) used in the assay (X axis) vs. % specific lysis (Y axis). The results indicate that humanized 12G6 antibodies 12G6-SFD1/K11 and 12G6-SFD1/K12 mediated equivalent ADCC killing as compared to the 12G6 chimeric antibody. The IgG1 isotype control showed only low levels of background killing at the concentrations tested.

Example 36: Assessment of the CDC Activities of Chimeric and Humanized 12G6 Monoclonal Antibodies

Humanized and chimeric 12G6 antibodies were evaluated for their ability to mediate complement dependent cytotoxicity (CDC) of CD52 expressing cells. A CDC assay was carried out by chromium release assays using T cells isolated from healthy donor PBMCs as target cells, as described above in Example 32. FIG. 40 illustrates the concentrations of control IgG, chimeric 12G6 antibody, and humanized 12G6 antibodies (12G6-SFD1/K11 and 12G6-SFD1/K12) used in the assay (X axis) vs. % specific lysis (Y axis). The results indicate that the chimeric 12G6 antibody mediated equivalent lysis as compared to humanized 12G6 antibodies (12G6-SFD1/K11 and 12G6-SFD1/K12). The control IgG1 isotype antibody showed only low levels of background killing at the concentrations tested.

Example 37: Assessment of the ADCC Activities of Chimeric and Humanized 9D9 Monoclonal Antibodies

Humanized and chimeric 9D9 antibodies were evaluated for their ability to mediate ADCC killing of CD52 expressing cells. An ADCC assay was carried out by chromium release assays using T cells isolated from healthy donor PBMCs as target cells, as described above in Example 31. FIG. 41 illustrates the concentrations of control IgG, chimeric 9D9 antibody, and humanized 9D9 antibodies (9D9-H10/K13, 9D9-H11/K13, 9D9-H16/K13, and 9D9-H18/K13) used in the assay (X axis) vs. % specific lysis (Y axis). The results indicate that the chimeric and humanized 9D9 antibodies (with the exception of 9D9-H10/K13) mediated equivalent ADCC killing. The IgG1 isotype control showed only low levels of background killing at the concentrations tested.

Example 38: Assessment of the CDC Activities of Chimeric and Humanized 9D9 Monoclonal Antibodies

Humanized and chimeric 9D9 antibodies were evaluated for their ability to mediate complement dependent cytotoxicity (CDC) of CD52 expressing cells. A CDC assay was carried out by chromium release assays using T cells isolated from healthy donor PBMCs as target cells, as described above in Example 32. FIG. 42 illustrates the concentrations of control IgG, chimeric 9D9 antibody, and humanized 9D9 antibodies (9D9-H10/K13, 9D9-H11/K13, 9D9-H16/K13, and 9D9-H18/K13) used in the assay (X axis) vs. % specific lysis (Y axis). The results indicate that a chimeric 9D9 antibody mediated equivalent lysis as compared to humanized 9D9 antibodies (with the exception of 9D9-H10/K13). The control IgG1 isotype antibody showed only low levels of background killing at the concentrations tested.

Example 39: Assessment of the ADCC Activities of Campath-1H® and Humanized Anti-CD52 Antibodies on Primary T Cells

Campath-1H® and humanized anti-CD52 antibodies were evaluated for their ability to mediate ADCC killing of CD52 expressing cells. An ADCC assay was carried out by chromium release assays using T cells isolated from healthy donor PBMCs as target cells, as described above in Example 31. FIG. 43 illustrates the concentrations of control IgG, Campath-1H®, and humanized 2C3-SFD1/K12, 9D9-H16/K13, 9D9-H18/K13, 12G6-SFD1/K11, and 12G6-SFD1/K12 antibodies used in the assay (X axis) vs. % specific lysis (Y axis). The results indicate that the above humanized 2C3, 9D9, and 12G6 antibodies mediated ADCC killing equivalent to that of Campath-1H® at concentrations in excess of 10 ng/ml. The IgG1 isotype control showed only low levels of background killing at the concentrations tested.

Example 40: Assessment of the CDC Activities of Campath-1H® and Humanized Anti-CD52 Antibodies on Primary T Cells

Campath-1H® and humanized anti-CD52 antibodies were evaluated for their ability to mediate complement dependent cytotoxicity (CDC) of CD52 expressing cells. A CDC assay was carried out by chromium release assays using T cells isolated from healthy donor PBMCs as target cells, as described above in Example 32. FIG. 44 illustrates the concentrations of control IgG, Campath-1H®, and humanized 2C3-SFD1/K12, 9D9-H16/K13, 9D9-H18/K13, 12G6-SFD1/K11, and 12G6-SFD1/K12 antibodies used in the assay (X axis) vs. % specific lysis (Y axis). The results indicate that humanized 2C3 and 12G6 antibodies mediated CDC killing equivalent to Campath-1H®, while humanized 9D9 antibodies demonstrated significantly reduced CDC activity, similar to their corresponding chimeric antibody. The IgG1 isotype control showed only low levels of background killing at the concentrations tested.

Example 41: Assessment of Neutralizing Ability of Serum Samples Containing Anti-Campath-1H® Neutralizing Antibodies to Block Humanized 2C3, 12G6, and 9D9 Anti-CD52 Antibody Activity

To assess the ability of humanized antibodies to bind to CD52 expressing cells in the presence of neutralizing antibodies against Campath-1H®, anti-CD52 antibodies (Campath-1H®, 2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12) were reacted with human serum containing anti-Campath-1H® antibody reactivity and evaluated for binding to CD52 expressing Raji cells. Serum samples obtained from relapsing remitting multiple sclerosis patients who were enrolled in the CAMMS223 study (The CAMMS223 Trial Investigators, “Alemtuzumab vs. interferon Beta-1a in early multiple sclerosis,” N Engl J Med 359:1786-1801 (2008)) were used in the assay. Repeated administration of the Campath-1H® antibody resulted in generation of anti-Campath-1H® antibody responses in most patients. The anti-Campath-1H antibody titer is very low at month 12 in most patients, and increased significantly upon administration of a second cycle of Campath-1H® resulting in a high titer anti-Campath-1H® response in the sera at month 13. Anti-CD52 antibody neutralization assays were carried out using month 12 and month 13 serum samples obtained from five different MS patients (MS-1 to MS-5) who had been treated with Campath-1H® under the CAMMS223 protocol. FITC-conjugated anti-CD52 antibodies Campath-1H®, 2C3-SFD1/K12, 12G6-SFD1/K12, and 9D9-H16/K13 (used in Example 30 and shown to bind to CD52 expressing cells) were used to stain Raji cells that express human CD52 in the absence or presence of a range of dilutions of serum obtained from patients who have been treated with Campath-1H. Briefly, MS patient serum samples (month 12 and month 13) were made into 6 fold serial dilutions and incubated with 10 μg/ml of FITC-conjugated anti-CD52 antibodies (Campath-1H®, 2C3-SFD1/K12, 12G6-SFD1/K12, and 9D9-H16/K13) for 1 hr at 37° C. Raji cells were rinsed with a staining buffer containing HBSS, 5% FBS, and 0.1% azide, and then deposited into round-bottom 96 well plates at 1×10⁵ cells per well. Cells were blocked with 10 μg/ml of human IgG Fc fragment for 30 min on ice in staining buffer. The cells were then washed with staining buffer and re-suspended in 100 μl of the antibody-serum mix as described above. After 30 minutes on ice, cells were washed and fixed with BD Cytofix and the FITC-labeled antibody coated cells were analyzed using a FACSCalibur system (Becton Dickinson), after which the data was analyzed using FlowJo version 7.2 software (Tree Star, Inc, Oregon, USA). Binding of FITC-conjugated anti-CD52 antibodies in the presence of anti-Campath-1H® neutralizing antibodies in the serum was assessed by flow cytometry and % binding relative to control, as a measure of inhibition was calculated as (MFI with serum/MFI control (no serum))×100. Representative data from one of the donors (MS-1) is shown in FIG. 45. The X axis denotes the serum dilution factor and the Y axis denotes the % control binding as a measure of antibody neutralizing activity. The data clearly demonstrate that month 12 serum samples have no inhibitory effect on Campath-1H® or other anti-CD52 antibodies, suggesting that there are low or no anti-Campath-1H® blocking antibodies in the serum. Month 13 serum samples mediated complete inhibition of Campath-1H® binding even at a 1:1000 dilution of serum, but did not mediate inhibition of 2C3, 12G6, and 9D9 humanized anti-CD52 antibodies even at the highest concentration (1:24 dilution) tested. Two of the five patients developed anti-Campath-1H® neutralizing antibody titers of >1:1000, whereas three other patients had about 1:100 Campath-1H® neutralizing antibody titers. Even though two of the patients' month 13 sera had relatively high neutralizing antibody titers of >1:1000 against Campath-1H®, these sera did not inhibit binding of humanized 2C3-SFD1/K12, 12G6-SFD1/K12, and 9D9-H16/K13 antibodies, suggesting that the anti-Campath-1H® antibody reactivity in patients treated with Campath-1H® did not block binding of these humanized antibodies to CD52 as presented on cells.

Example 42: Analysis of Depletion and Repopulation of Anti-CD52 Antibodies in huCD52 Transgenic Mice (4B10-H1/K1)

The depleting activities of Campath-1H® and the humanized anti-CD52 antibody (4B10-H1/K1) at different dose levels were examined in the huCD52 transgenic mouse. Mice were injected intravenously with 0.1, 0.5, 1.0 or 5.0 mg/kg of each antibody. Two hours post dosing, serum was collected to examine the level of circulating cytokines. Three days post dosing, mice were sacrificed, and blood and spleens were collected from each mouse (N=5) to determine the level of cell depletion using flow cytometry analysis. Samples were evaluated to determine the relative numbers of total T helper cell (CD4+), cytotoxic T cell (CD8+), B cell (B220+) and myeloid cell subpopulations present in the circulating peripheral blood or spleen of huCD52 transgenic mice. In addition, T and B cell subset analysis was performed to determine the overall depleting effect. A subset of mice (N=5) were kept alive to monitor the repopulation kinetics. Depletion was greatest in the T cell compartment with CD4+ T cells being depleted most followed by CD8+ T cells, B cells, NK cells, and other myeloid cells. Within the CD4+ T cell compartment, naïve CD4+ T cells were depleted the most followed by CD4+ central memory (CM), CD4+ effector memory (EM), and CD4+ regulatory T cells (Treg). A similar pattern was observed for CD8+ T cells (Naïve>CM>EM). Conversely, mature B cells were depleted to a greater extent than immature B cells. Comparison of Campath-1H® treated mice to 4B10-H1/K1 treated mice demonstrated similar patterns of cells in both the blood and spleen at each of the doses examined.

Serum cytokine analysis demonstrated dose dependent increases for TNFα, IL-6 and MCP-1. The circulating level of these cytokines remained elevated compared to untreated mice at the 0.5 and 0.1 mg/kg doses as well. Slight increases were also observed for IL-10 in the Campath-1H® treated group at the three highest doses but only for the highest dose of the humanized 4B10-H1/K1 treated group. No significant increases in the level of circulating IL-12 or IFNg (not shown) were noted.

By 50-60 days post dosing, with the exception of the 1.0 mg/kg group, lymphocyte levels in all of the Campath-1H® dosed groups had rebounded to the levels of untreated mice. In the 1.0 mg/kg group, lymphocytes had returned to normal levels by 80 days post dosing. Similar repopulation kinetics were also observed for the humanized 4B10-H1/K1 antibody treated mice. Lymphocytes had rebounded to control levels by 50 days post dosing in all 4B10-H1/K1 treated groups with the exception of the 0.5 mg/kg level. Levels of circulating lymphocytes in the 0.5 mg/kg group remained decreased throughout the course of the monitoring period. Total lymphocytes were monitored for repopulation in the blood.

FIGS. 46A-46E show the level of CD4+ T cells, CD8+ T cells and B220+ B cells in the blood 72 hours after dosing with Campath-1H® (“Campath”) and humanized 4B10-H1/K1 (“4B10”) antibodies. FIGS. 47A-47E show the level of CD4+ T cells, CD8+ T cells and B220+ B cells in the spleen 72 hours after dosing with Campath-1H® (“Campath”) and humanized 4B10-H1/K1 (“4B10”) antibodies. FIGS. 48A-48E show the levels of circulating cytokines 2 hours after dosing with Campath-1H® (“Campath”) and humanized 4B10-H1/K1 (“4B10”) antibodies. FIGS. 49A-49B show the repopulation of circulating lymphocytes over a timecourse after dosing with Campath-1H® (“Campath”) and humanized 4B10-H1/K1 (“4B10”) antibodies.

Example 43: Analysis of Depletion and Repopulation of Anti-CD52 Antibodies in huCD52 Transgenic Mice (7F11-SFD1/K2 and 7F11-SFD2/K2)

The depleting activity of humanized antibodies (7F11-SFD1/K2 and 7F11-SFD2/K2) at different dose levels was examined in huCD52 transgenic mice. Mice were injected intravenously with 0.1, 0.5, 1.0 or 5.0 mg/kg of each antibody. Two hours post dosing, serum was collected to examine the level of circulating cytokines. Three days post dosing, mice were sacrificed, and blood and spleens were collected from each mouse (N=5) to determine the level of cell depletion using flow cytometry analysis. Samples were evaluated to determine the relative numbers of total T helper cell (CD4+), cytotoxic T cell (CD8+), B cell (B220+) and myeloid cell subpopulations present in the circulating peripheral blood or spleen of huCD52 transgenic mice In addition, T and B cell subset analysis was performed to determine the overall depleting effect. A subset of mice (N=5) were kept alive to monitor the repopulation kinetics. Administration of each humanized 7F11 antibody (7F11-SFD1/K2 and 7F11-SFD2/K2) at all doses resulted in depletion of a significant number of both T cells and B cells in the blood. These data also demonstrated that various T and B cell subsets are depleted to differing degrees depending on the dose of antibody used. Naïve T cells (both CD4 and CD8) demonstrated the most depletion with other cell populations (including memory and T reg cells) being depleted to a lesser degree. In the B cell compartment, mature B cells were depleted more readily than immature B cells. In the spleen, dose dependent depletion was observed with significant depletion of lymphocytes being observed at the 5 and 1 mg/kg dose levels. Similar to the case with blood, naïve T cells were more readily depleted than memory cells. B cells were depleted to a lesser extent than T cells with each of the humanized 7F11 clones (7F11-SFD1/K2 and 7F11-SFD2/K2). Depletion was not observed for NK cells or neutrophils in the blood or the spleen at any of the doses injected. Serum cytokine analysis demonstrated dose dependent increases for both TNFα and IL-6. Levels of these cytokines remained elevated compared to untreated mice at the 0.5 and 0.1 mg/kg doses as well. Dose dependent increases in the level of circulating MCP-1 were also noted.

By 30 days post dosing, lymphocyte levels in the 0.5 and 0.1 mg/kg dosed groups had rebounded to the levels of untreated mice. In the 1.0 and 5.0 mg/kg groups, lymphocytes had returned to normal levels by 50 and 80 days, respectively, for clone 7F11-SFD1/K2 and by 80 days post dosing for both the 1.0 and 5.0 mg/kg groups of clone 7F11-SFD2/K2. Total lymphocytes were monitored for repopulation in the blood.

FIGS. 50A-50E show the level of CD4+ T cells, CD8+ T cells and B220+ B cells in the blood 72 hours after dosing with the humanized 7F11-SFD1/K2 (“7F11 SFD1”) and 7F11-SFD2/K2 (“7F11 SFD2”) antibodies. FIGS. 51A-51E show the level of CD4+ T cells, CD8+ T cells and B220+ B cells in the spleen 72 hours after dosing with the humanized 7F11-SFD1/K2 (“7F11 SFD1”) and 7F11-SFD2/K2 (“7F11 SFD2”) antibodies. FIGS. 52A-52F show the levels of circulating cytokines 2 hours after dosing with the humanized 7F11-SFD1/K2 (“7F11 SFD1”) and 7F11-SFD2/K2 (“7F11 SFD2”) antibodies. FIGS. 53A-53B show the repopulation of circulating lymphocytes over a timecourse after dosing with the humanized 7F11-SFD1/K2 (“7F11 SFD1”) and 7F11-SFD2/K2 (“7F11 SFD2”) antibodies.

Example 44: Analysis of 7F11 Humanized Anti-CD52 Antibodies in CD52 Transgenic Mice (7F11-SFD1/K2 and 7F11-SFD2/K2)

The depleting activity of the chimeric 7F11 antibodies and humanized 7F11-SFD1/K2 and 7F11-SFD2/K2 antibodies in comparison to Campath-1H® was examined in the huCD52 transgenic mouse. Mice were injected intravenously with 1.0 mg/kg of each antibody. Three days post dosing, mice were sacrificed, and blood and spleens were collected from each mouse (N=5) to determine the level of cell depletion using flow cytometry analysis. Samples were evaluated to determine the relative numbers of total T helper cell (CD4+), cytotoxic T cell (CD8+), B cell (B220+) and myeloid cell subpopulations present in the circulating peripheral blood or spleen of huCD52 transgenic mice. Administration of Campath-1H® resulted in depletion of a significant number of both T cells and B cells in the blood and spleen. Although a comparable level of T cell depletion was observed in the blood for both the chimeric and humanized 7F11 antibodies (7F11-SFD1/K2 and 7F11-SFD2/K2), B cells were depleted to a lesser extent. This observation was also apparent in the spleen, where significant T cell depletion was noted, but only a modest level of B cell depletion was achieved with the 7F11 antibodies (7F11-SFD1/K2 and 7F11-SFD2/K2).

FIGS. 54A-54B show the level of CD4+ T cells, CD8+ T cells and B220+ B cells in the blood 72 hours after dosing with Campath-1H® (“Campath”), 7F11-chimeric antibodies, and humanized 7F11-SFD1/K2 and 7F11-SFD2/K2 antibodies.

Example 45: Analysis of PK Profiles of Anti-CD52 Antibodies in CD52 Transgenic Mice (7F11-SFD1/K2 and 7F11-SFD2/K2)

To ensure that the humanization process did not alter the clearance rate of the antibody, the pharmacokinetic profile of the chimeric 7F11 anti-CD52 antibody and humanized 7F11-SFD1/K2 and 7F11-SFD2/K2 anti-CD52 antibodies was determined in huCD52 transgenic mice. Mice were injected intravenously with antibodies at 5 mg/kg and blood was collected at various timepoints beginning two hours post dosing. The circulating levels of each antibody were evaluated using an anti-human IgG ELISA. For each of the humanized clones, there was a slight difference in the Cmax noted at 2 hours post dosing. Clearance rates for the chimeric 7F11 antibody and humanized 7F11-SFD1/K2 and 7F11-SFD2/K2 antibodies were similar to each other as well as to Campath-1H® over the course of the experiment, indicating that the humanization process did not significantly alter the pharmacokinetic profile of the antibodies.

FIG. 55 shows the level of Campath-1H® (“Campath”), 7F11-chimeric antibody and humanized 7F11-SFD1/K2 and 7F11-SFD2/K2 antibodies in the blood over a timecourse after dosing.

Example 46: Analysis of Depletion and Repopulation of Anti-CD52 Antibodies in huCD52 Transgenic Mice (2C3-SFD1/K12)

The depleting activity of the 2C3-SFD1/K12 clone at different dose levels was examined in the huCD52 transgenic mouse. Mice were injected intravenously with 0.1, 0.5, 1.0 or 5.0 mg/kg of antibody. Two hours post dosing, serum was collected to potentially examine the level of circulating cytokines. Three days post dosing, mice were sacrificed, and blood and spleens were collected from each mouse (N=5) to determine the level of cell depletion using flow cytometry analysis. Samples were evaluated to determine the relative numbers of total T helper cell (CD4+), cytotoxic T cell (CD8+), B cell (B220+) and myeloid cell subpopulations present in the circulating peripheral blood or spleen of huCD52 transgenic mice. In addition, T and B cell subset analysis was performed to determine the overall depleting effect. A subset of mice (N=5) were kept alive to monitor the repopulation kinetics. Administration of 2C3-SFD1/K12 at the 5, 1, and 0.5 mg/kg doses resulted in depletion of a significant number of both T cells and B cells in the blood. A variable level of lymphocyte depletion was observed in the blood at the 0.1 mg/kg dose with CD4+ T cells and B cells being depleted to a greater extent than CD8+ T cells. These data also demonstrated that various T and B cell subsets are depleted to differing degrees depending on the dose of antibody used. Naïve T cells (both CD4 and CD8) demonstrated the most depletion compared to other cell populations (including memory and T reg cells), which were depleted to a lesser degree. In the B cell compartment, mature B cells were depleted more readily than immature B cells. In the spleen, dose dependent depletion was observed with significant depletion of lymphocytes being observed at the 5 and 1 mg/kg dose levels. Similar to Campath-1H®, naïve T cells were more readily depleted than memory cells. Depletion was observed for NK cells and neutrophils in the blood, but little to no depletion was observed in the spleen at any of the doses injected. Serum cytokine analysis demonstrated dose dependent increases for both TNFα and IL-6 with the 5 mg/kg dose inducing the highest level of each cytokine. Levels comparable to untreated mice were observed in the 0.5 and 0.1 mg/kg dose levels for TNFα and the 0.1 mg/kg dose level for IL-6. Dose dependent increases in the level of circulating MCP-1 were also noted.

By 30 days post dosing, lymphocyte levels for the 0.1 and 0.5 mg/kg groups had rebounded to the levels of untreated mice. In the 1.0 and 5.0 mg/kg groups, lymphocytes had returned to normal levels by 80 days post dosing. Total lymphocytes were monitored for repopulation in the blood.

FIGS. 56A-56E show the level of CD4+ T cells, CD8+ T cells and B220 B cells in the blood 72 hours after dosing with 2C3-SFD1/K12 antibodies. FIGS. 57A-57E show the level of CD4+ T cells, CD8+ T cells and B220+ B cells in the spleen 72 hours after dosing with 2C3-SFD1/K12 antibodies. FIGS. 58A-58F show the levels of circulating cytokines 2 hours after dosing with 2C3-SFD1/K12 antibodies. FIG. 59 shows the repopulation of circulating lymphocytes over a timecourse after dosing with 2C3-SFD1/K12 antibodies.

Example 47: Analysis of Depletion and Repopulation of Anti-CD52 Antibodies in huCD52 Transgenic Mice (12G6-SFD1/K11)

The depleting activity of the 12G6-SFD1/K11 clone at different dose levels was examined in the huCD52 transgenic mouse. Mice were injected intravenously with 0.1, 0.5, 1.0 or 5.0 mg/kg of antibody. Two hours post dosing, serum was collected to potentially examine the level of circulating cytokines. Three days post dosing, mice were sacrificed, and blood and spleens were collected from each mouse (N=5) to determine the level of cell depletion using flow cytometry analysis. Samples were evaluated to determine the relative numbers of total T helper cell (CD4+), cytotoxic T cell (CD8+), B cell (B220+) and myeloid cell subpopulations present in the circulating peripheral blood or spleen of huCD52 transgenic mice. In addition, T and B cell subset analysis was performed to determine the overall depleting effect. A subset of mice (N=5) were kept alive to monitor the repopulation kinetics. Administration of 12G6-SFD1/K11 at the 5, 1, and 0.5 mg/kg doses resulted in depletion of a significant number of both T cells and B cells in the blood. A variable level of lymphocyte depletion was observed in the blood at the 0.1 mg/kg dose with CD4+ T cells and B cells being depleted to a greater extent than CD8+ T cells. These data also demonstrated that various T and B cell subsets are depleted to differing degrees depending on the dose of antibody used. Naïve T cells (both CD4 and CD8) demonstrated the most depletion compared to other cell populations (including memory and T reg cells), which were depleted to a lesser degree. In the B cell compartment, mature B cells were depleted more readily than immature B cells. In the spleen, dose dependent depletion was observed with significant depletion of lymphocytes being observed at the 5 and 1 mg/kg dose levels. Similar to Campath-1H®, naïve T cells were more readily depleted than memory cells. Depletion was observed for NK cells and neutrophils in the blood but little to no depletion was observed in the spleen at any of the doses injected. Serum cytokine analysis demonstrated dose dependent increases for both TNFα and IL-6 with the 5 mg/kg dose inducing the highest level of each cytokine. Levels comparable to untreated mice were observed in the 0.5 and 0.1 mg/kg dose levels for TNFα and the 0.1 mg/kg dose level for IL-6. Dose dependent increases in the level of circulating MCP-1 were also noted.

By 30 days post dosing, lymphocyte levels had rebounded to the levels of untreated mice. In the 1.0 and 5.0 mg/kg groups, lymphocytes had returned to normal levels by 80 days post dosing. Total lymphocytes were monitored for repopulation in the blood.

FIGS. 60A-60E show the level of CD4+ T cells, CD8+ T cells and B220+ B cells in the blood 72 hours after dosing with 12G6-SFD1/K11 antibodies. FIGS. 61A-61E show the level of CD4+ T cells, CD8+ T cells and B220+ B cells in the spleen 72 hours after dosing with 12G6-SFD1/K11 antibodies. FIGS. 62A-62F show the levels of circulating cytokines 2 hours after dosing with 12G6-SFD1/K11 (“12G6 hu”) antibodies. FIG. 63 shows the repopulation of circulating lymphocytes over a timecourse after dosing with 12G6-SFD1/K11 antibodies.

Example 48: Analysis of PK Profile of Anti-CD52 Antibodies in CD52 Transgenic Mice (2C3-SFD1/K12, 12G6-SFD1/K11 and 9D9-H10/K12)

The pharmacokinetic profiles of anti-CD52 antibodies were determined in huCD52 transgenic mice. This experiment compared the humanized and chimeric forms of the antibodies to ensure that the humanization process did not alter the clearance rate of the antibodies. Comparisons included chimeric 2C3, 12G6, and 9D9 antibodies and humanized 2C3-SFD1/K12, 12G6-SFD1/K11, and 9D9-H10/K12 antibodies. Mice were injected i.v. with antibodies at 5 mg/kg and blood was collected at various timepoints beginning two hours post dosing. The circulating levels of each antibody were evaluated using an anti-human IgG ELISA. For each of the chimeric/humanized antibody pairs analyzed, there was a slight difference in the Cmax noted at 2 hours post dosing. For the 2C3 and 12G6 antibodies, the Cmax of the humanized version (i.e., 2C3-SFD1/K12 and 12G6-SFD1/K11) was slightly higher while the chimeric version was slightly higher for the 9D9 pair. Clearance rates for the antibody pairs were similar over the course of the experiment indicating that the humanization process did not significantly alter the pharmacokinetic profile of the antibodies.

FIGS. 64A-64C show the level of 2C3-chimeric, 2C3-SFD1/K12, 12G6-chimeric, 12G6-SFD1/K11, 9D9-chimeric, and 9D9-H10/K12 antibodies in the blood over a timecourse after dosing.

Example 49: Analysis of Depletion and Repopulation of Anti-CD52 Antibodies in huCD52 Transgenic Mice (9D9-H10/K12)

The depleting activity of the 9D9-H10/K12 clone at different dose levels was examined in the huCD52 transgenic mouse. Mice were injected intravenously with 0.1, 0.5, 1.0 or 5.0 mg/kg of antibody. Two hours post dosing, serum was collected to potentially examine the level of circulating cytokines. Three days post dosing, mice were sacrificed, and blood and spleens were collected from each mouse (N=5) to determine the level of cell depletion using flow cytometry analysis. Samples were evaluated to determine the relative numbers of total T helper cell (CD4+), cytotoxic T cell (CD8+), B cell (B220+) and myeloid cell subpopulations present in the circulating peripheral blood or spleen of huCD52 transgenic mice. In addition, T and B cell subset analysis was performed to determine the overall depleting effect. A subset of mice (N=5) were kept alive to monitor the repopulation kinetics. Administration of 9D9-H10/K12 at the 5, 1, and 0.5 mg/kg doses resulted in depletion of a significant number of both T cells and B cells in the blood. Only a modest level of lymphocyte depletion was observed in the blood at the 0.1 mg/kg dose. These data also demonstrated that various T and B cell subsets are depleted to differing degrees depending on the dose of antibody used. Naïve T cells (both CD4 and CD8) demonstrated the most depletion compared to other cell populations (including memory and T reg cells), which were depleted to a lesser degree. In the B cell compartment, mature B cells were depleted more readily than immature B cells. In the spleen, significant depletion of these cells was only observed at the 5 and 1 mg/kg dose levels. Similar to Campath-1H®, naïve T cells were more readily depleted than memory cells. Depletion was observed for NK cells and neutrophils in the blood but little to no depletion was observed in the spleen at any of the doses injected. Serum cytokine analysis demonstrated no significant increases for either TNFα or IL-6 at any of the dose levels analyzed. Dose dependent increases in the level of circulating MCP-1, however, were noted.

The repopulation portion of this experiment was terminated early when lymphocytes were 50-80% repopulated (depending on the dose). Lymphocyte repopulation was monitored based on total lymphocyte counts and not on a T and B cell basis.

FIGS. 65A-65E show the level of CD4+ T cells, CD8+ T cells and B220+ B cells in the blood 72 hours after dosing with 9D9-H10/K12 (“9D9”) antibodies. FIGS. 66A-66E show the level of CD4+ T cells, CD8+ T cells and B220+ B cells in the spleen 72 hours after dosing with 9D9-H10/K12 (“9D9”) antibodies. FIGS. 67A-67F show the levels of circulating cytokines 2 hours after dosing with 9D9-H10/K12 (“9D9”) antibodies. FIG. 68 shows the repopulation of circulating lymphocytes over a timecourse after dosing with 9D9-H10/K12 (“9D9”) antibodies.

Example 50: Analysis of Depletion and Repopulation of Anti-CD52 Antibodies in huCD52 Transgenic Mice (2C3-SFD1/K12, 12G6-SFD1/K11 and 9D9-H10/K12)

The depleting activity of Campath-1H® and the humanized 2C3-SFD1/K12, 12G6-SFD1/K11 and 9D9-H10/K12 clones at different dose levels was examined in the huCD52 transgenic mouse. Mice were injected intravenously with either 0.1 or 1.0 mg/kg of antibody. Two hours post dosing, serum was collected to potentially examine the level of circulating cytokines. Three days post dosing, mice were sacrificed, and blood and spleens were collected from each mouse to determine the level of cell depletion using flow cytometry analysis. Samples were evaluated to determine the relative numbers of total T helper cell (CD4+), cytotoxic T cell (CD8+), B cell (B220+) and myeloid cell subpopulations present in the circulating peripheral blood or spleen of huCD52 transgenic mice. In addition, T and B cell subset analysis was performed to determine the overall depleting effect. All of the humanized antibodies (2C3-SFD1/K12, 12G6-SFD1/K11 and 9D9-H10/K12) mediated depletion of lymphocytes within the spleen and blood when compared with PBS treated animals. Depletion was more robust in the blood than the spleen for all antibodies, and the depletion was dose-dependent in both tissues. Depletion was most dramatic for CD4 and CD8+ T cells with less depletion in the B cell compartment. Various T and B cell subsets were depleted to differing degrees. Naïve T cells (both CD4 and CD8) demonstrated the most depletion compared to other cell populations (including memory and T reg cells), which were depleted to a lesser degree. In the B cell compartment, mature B cells were depleted more readily than immature B cells. Serum cytokine analysis revealed significant increases in the level of IL-6, MCP-1 and TNFα 2 hours post dosing. Increases were noted for all antibodies, including Campath-1H®, and were dose dependent (i.e. higher cytokine levels were noted for the 1.0 mg/kg dose level than the 0.1 mg/kg dose). In comparison to Campath-1H®, 2C3-SFD1/K12 and 12G6-SFD1/K11 induced similar levels of IL-6 while 9D9-H10/K12 induced IL-6 to a significantly lower degree. For MCP-1, the 12G6-SFD1/K11 antibody induced lower levels, and both 12G6-SFD1/K11 and 9D9-H10/K12 decreased TNFα levels compared to Campath-1H®.

FIGS. 69A-69D show the level of bulk lymphocyte populations (CD4+ T cells, CD8+ T cells, and B cells) and CD4+ T cell, CD8+ T cell and B220+B/NK cell subtypes in the blood 72 hours after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12 (“2C3”), 12G6-SFD1/K11 (“12G6”), and 9D9-H10/K12 (“9D9”) antibodies. FIGS. 70A-70D show the level of bulk lymphocyte populations (CD4+ T cells, CD8+ T cells, and B cells) and CD4+ T cell, CD8+ T cell and B220+B/NK cell subtypes in the spleen 72 hours after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12 (“2C3”), 12G6-SFD1/K11 (“12G6”), and 9D9-H10/K12 (“9D9”) antibodies. FIGS. 71A-71F show the levels of circulating cytokines 2 hours after dosing with Campath-1H®, 2C3-SFD1/K12, 12G6-SFD1/K11, and 9D9-H10/K12 antibodies.

Example 51: Direct Comparison of Anti-huCD52 Humanized 9D9 Clones in huCD52 Transgenic Mice (9D9 H10/K12 and 9D9 H11/K12)

The depleting activity of two humanized anti-CD52 9D9 clones (9D9-H10/K12 and 9D9-H11/K12) was examined in huCD52 transgenic mice. Mice were injected intravenously with either 0.1 or 1.0 mg/kg of antibody. Three days post dosing, mice were sacrificed, and blood and spleens were collected from each mouse to determine the level of cell depletion using flow cytometry analysis. Samples were evaluated to determine the relative numbers of total T helper cell (CD4+), cytotoxic T cell (CD8+), B cell (B2200+) and NK cell subpopulations present in the circulating peripheral blood or spleen of huCD52 transgenic mice. Treatment with either antibody resulted in similar lymphocyte depletion within the blood and spleen, with lymphocyte depletion in the blood being more robust. Further, CD4 and CD8+ T cells were more strongly depleted than B cells and NK cells in both tissues. While the depletion with the 9D9-H10/K12 clone appears less robust than the depletion with the 9D9-H11/K12 clone, the difference is not statistically significant.

FIG. 72 shows the level of CD4+ T cells, CD8+ T cells, B220+ B cells, and NK cells in the blood 72 hours after dosing with 9D9-H10/K12 and 9D9-H11/K12 antibodies. FIG. 73 shows the level of CD4+ T cells, CD8+ T cells, B220+ B cells, and NK cells in the spleen 72 hours after dosing with 9D9-H10/K12 and 9D9-H11/1(12 antibodies.

Example 52: Direct Comparison of Anti-huCD52 Humanized 12G6 Clones in huCD52 Transgenic Mice (12G6-SFD1/K11 and 12G6-SFD1-K12)

The depleting activity of two humanized anti-CD52 12G6 clones (12G6-SFD1/K11 and 12G6-SFD1/K12) was examined in the huCD52 transgenic mouse. Mice were injected intravenously with either 0.1 or 1.0 mg/kg of antibody. Two hours post dosing, serum was collected to potentially examine the level of circulating cytokines. Three days post dosing, mice were sacrificed, and blood and spleens were collected from each mouse to determine the level of cell depletion using flow cytometry analysis. Samples were evaluated to determine the relative numbers of total T helper cell (CD4+), cytotoxic T cell (CD8+), B cell (B220+) and myeloid cell subpopulations present in the circulating peripheral blood or spleen of huCD52 transgenic mice. In addition, T and B cell subset analysis was performed to determine the overall depleting effect. Administration of either the 12G6-SFD1/K11 antibody or the 12G6-SFD1/K12 antibody resulted in a significant level of lymphocyte depletion within the blood. There appeared to be little to no difference in the lymphocyte depleting activity of the two clones. The pattern of lymphocyte depletion was s such that naïve CD4 and CD8+ T cells were depleted to a higher degree than memory T cells or Treg cells. Myeloid cell populations were depleted to a lesser degree regardless of the clone (12G6-SFD1/K11 or 12G6-SFD1/K12) or dose. Serum cytokine analysis was not performed for this experiment.

FIGS. 74A-74D show the level of CD4+ T cells, CD8+ T cells, B220+B/NK cells, and myeloid cells in the blood 72 hours after dosing with 12G6-SFD1/K11 (“12G6 K11”) and 12G6-SFD1/K12 (“12G6 K12”) antibodies. FIGS. 75A-75D show the level of CD4+ T cells, CD8+ T cells, B220+B/NK cells, and myeloid cells in the spleen 72 hours after dosing with 12G6-SFD1/K11 (“12G6 K11”) and 12G6-SFD1/K12 (“12G6 K12”) antibodies.

Example 53: Direct Comparison of Anti-huCD52 Humanized 9D9 Clones in huCD52 Transgenic Mice (9D9 H11/K12, 9D9 H16/K13, and 9D9 H18/K13)

The depleting activity of three humanized 9D9 antibodies (9D9-H11/K12, 9D9-H16/K13, and 9D9-H18/K13) was compared in the huCD52 transgenic mouse. Human CD52 transgenic mice were treated with PBS as a vehicle control or injected with either 1 mg/kg or 0.1 mg/kg of each antibody. At two hours post dosing, serum was collected to determine the level of circulating cytokines. Three days later, mice were sacrificed, and peripheral blood and spleens were collected and processed for flow cytometry analysis. Samples were evaluated to determine the relative numbers of total T helper cell (CD4+), cytotoxic T cell (CD8+), B cell (B220+) and myeloid cell subpopulations present in the circulating peripheral blood or spleen of huCD52 transgenic mice. In addition, T and B cell subset analysis was performed to determine the overall depleting effect. All 9D9 (9D9-H11/K12, 9D9-H16/K13, and 9D9-H18/K13) antibodies mediated cellular depletion of lymphocyte and myeloid cell populations in the blood and spleen to a similar extent. More robust lymphocyte and myeloid cell depletion was observed in the blood than the spleen. Comparison of the depleting activity of the 9D9 clones (9D9-H11/K12, 9D9-H16/K13, and 9D9-H18/K13) demonstrated that 9D9-H16/K13 resulted in the most robust depletion, followed by 9D9-H18/K13 and 9D9-H11/K12. This was most apparent for lymphocytes in the spleen at the 1 mg/kg dose in which 9D9-H16/K13 treatment resulted in a higher degree of depletion than either of the other clones (9D9-H18/K13 and 9D9-H11/K12). Further, the pattern of depletion was such that naïve CD4 and CD8+ T cells were depleted to a higher degree than memory T cells or Treg cells, and B cell populations were depleted to a higher level with 9D9-H16/K13. Myeloid cell populations were less impacted by anti-CD52 treatment regardless of the clone of antibody (9D9-H11/K12, 9D9-H16/K13, or 9D9-H18/K13) or dose. Of the cytokines analyzed, increases were noted in IL-6, TNFα and MCP-1. Following injection, similar circulating level of IL6 and MCP-1 were observed for all of the 9D9 clones (9D9-H11/K12, 9D9-H16/K13, and 9D9-H18/K13) at both the 0.1 and 1.0 mg/kg dose levels. Slight differences were observed with circulating TNFα levels in which injection of the 9D9-H16/K13 clone resulted in a modest increase at the 1.0 mg/kg dose.

FIG. 76 shows the level of bulk lymphocyte populations (CD4+ T cells, CD8+ T cells, and B220+ B cells) in the blood 72 hours after dosing with 9D9-H11/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies. FIGS. 77A-77D show the level of CD4+ T cell, CD8+ T cell, B220+B/NK cell, and myeloid cell subtypes in the blood 72 hours after dosing with 9D9-H11/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies. FIG. 78 shows the level of bulk lymphocyte populations (CD4+ T cells, CD8+ T cells, and B220+ B cells) in the spleen 72 hours after dosing with 9D9-H11/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies. FIGS. 79A-79D show the level of CD4+ T cell, CD8+ T cell, B220+B/NK cell, and myeloid cell subtypes in the spleen 72 hours after dosing with 9D9-H11/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies. FIGS. 80A-80F show the levels of circulating cytokines 2 hours after dosing with 9D9-H11/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies.

Example 54: Analysis of PK Profile of Anti-CD52 Antibodies from the 2C3, 12G6, and 9D9 Families in CD52 Transgenic Mice

The pharmacokinetic profiles of humanized 2C3-SFD1/K12, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13 and 9D9-H18/K13 were determined in huCD52 transgenic mice. Mice were injected i.v. with antibodies at 1 mg/kg and blood was collected at various timepoints beginning two hours post dosing. The circulating levels of each antibody were evaluated using an anti-human Ig ELISA. The calculated half-lives were: 2C3-SFD1/K12 79.0±23.9 hours, 12G6-SFD1/K11 49.0±14.4 hours, 12G6-SFD1/K12 75.1±28.5, 9D9-H16/K13 59.8+26.6 hours and 9D9-H18/K13 42.2+15.7 hours.

Overall, there was significant inter-animal variability for exposure in these studies. The terminal elimination half-lives for 2C3-SFD1/K12 and 12G6-SFD1/K12 were similar while the half-life of 12G6-SFD1/K11 was shorter but not significantly different. Clearance was fastest with 2C3-SFD1/K12 followed by 12G6-SFD1/K11 and 12G6-SFD1/K12. The two 12G6 treatments mirrored each other for most of the time points measured, while 2C3-SFD1/K12 showed less exposure and faster clearance. 9D9-H16/K13 and 9D9-H18/K13 were quite similar for all PK parameters measured.

FIGS. 81A-81B show the level of 2C3-SFD1/K12, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13 and 9D9-H18/K13 antibodies in the blood over a timecourse after dosing.

TABLE 16 PK Parameters 2C3-SFD1/K12 12G6-SFD1/K11 12G6-SFD1/K12 9D9-H16/K13 9D9-H18/K13 t_(1/2) (hr) 79.0 ± 23.9 49.0 ± 14.4 75.1 ± 28.5 59.8 ± 26.6 42.2 ± 15.7 Cl (ml/hr/kg) 20.3 ± 2.9  10.6 ± 1.69 7.08 ± 1.80 5.64 ± 1.73 6.65 ± 3.02 Vz (ml/kg) 2251 ± 539  770 ± 294 721 ± 224 445 ± 133 366 ± 100 AUC (ug*hr/ml)  251 ± 37.2 485 ± 104 747 ± 188  196 ± 70.2  174 ± 65.2 Cmax (ug/ml) 4.22 ± 0.54 7.12 ± 1.97 8.96 ± 2.33 3.58 ± 2.16 4.35 ± 1.54

Example 55: Evaluation of Cytokine Storm in Response to Treatment with Anti-CD52 Antibodies

The release of serum cytokine following treatment with anti-CD52 antibodies was evaluated in huCD52 transgenic mice. Animals were treated with 1 mg/kg of Campath-1H®, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13 or 9D9-H18/K13. One group of animals was treated with 5 mg/kg of 2C3-SFD1/K12 in view of previous results indicating that injection with 2C3-SFD1/K12 may result in lower levels of depletion compared to the other antibodies, thereby normalizing the groups based on the dose needed to achieve similar levels of depletion. All groups were bled 1 2, 4, 24, and 48 hours post treatment and CBA analysis for inflammatory cytokines was conducted. All groups were also sacrificed 3 days post treatment and the spleens were evaluated for depletion of lymphocytes in the spleen by flow cytometry. Treatment with each of the antibodies resulted in depletion of various targets similar to that observed for Campath-1H®. This was also true for 2C3-SFD1/K12, in which a 5 mg/kg dose was used to elicit similar depletion. Some variability in depletion was observed with 12G6-SFD1/K12 and 9D9-H16/K13, most likely due to the repeated bleeding of the animals to acquire serum for cytokine analysis. Cytokine expression, however, was reduced for antibodies from the 12G6 (12G6-SFD1/K11 and 12G6-SFD1/K12) and 9D9 (9D9-H16/K13 and 9D9-H18/K13) family members. This was most noticeable for release of IL-6, MCP-1 and TNFα at the early 1 and 2 hour time points.

FIGS. 82A-82F show the level of cytokines in the blood over a 48-hour timecourse following dosing with Campath-1H® (“Campath”), 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13 or 9D9-H18/K13 antibodies. FIGS. 83A-83E show the level of bulk lymphocytes, CD4+ T cells, CD8+ T cells, B220+B/NK cells, and myeloid cells in the spleen 72 hours after dosing with Campath-1H® (“Campath”), 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13 or 9D9-H18/K13 antibodies.

Example 56: Evaluation of the Repopulation Kinetics in the Blood of CD52 Transgenic Mice Following Treatment with Anti-CD52 Antibodies

The repopulation kinetics of several cell types in the blood were assessed following administration of humanized anti-CD52 2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12 antibodies. Mice were injected i.v. with each antibody at 2 mg/kg to ensure a robust level of depletion. At various timepoints post injection, blood was collected for flow cytometry analysis to determine the level of circulating lymphocytes in the blood, including CD4+ and CD8+ T cells, regulatory T cells, B cells, NK cells, neutrophils and macrophages. No differences were observed in the initial depleting activity for each antibody, which was confirmed on day 3 post injection. Mice were bled weekly for the first month and biweekly thereafter to monitor the kinetics of repopulation. The kinetics of lymphocyte repopulation were similar for any of the anti-CD52 (2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12) antibodies compared to Campath-1H®. By day 57, the B cells returned to baseline in the blood while T cells approached baseline levels by day 84. By day 116, CD8+ T cells had not returned to control levels, but similar repopulation kinetics for all other cell types monitored were observed with each of the anti-CD52 (2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12) antibodies and Campath-1H®.

FIGS. 84A-84G show the repopulation of circulating CD4+ and CD8+ T cells, regulatory T cells, B cells, NK cells, neutrophils and macrophages over a timecourse after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12 antibodies.

Example 57: Evaluation of CD52 Expression in CD52 Transgenic Mice Using the Anti-CD52 Antibodies

Expression of huCD52 was evaluated using the humanized anti-CD52 antibodies to determine whether similar staining patterns could be observed on mature and developing cell populations in huCD52 transgenic mice. 2C3-SFD1/K12, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies were conjugated with FITC to use in flow cytometry staining. Tissues from huCD52 transgenic mice were collected and processed for staining. 2C3-SFD1/K12, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies stained lymphocytes expressing huCD52 from the spleen of transgenic mice similar to Campath-1H®. The staining patterns were representative of the lymphocyte populations and subsets found in other lymphoid organs such as the thymus and bone marrow.

FIG. 85 shows the ability of FITC-labeled Campath-1H®, 2C3-SFD1/K12, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies to specifically bind huCD52 lymphocyte cell populations in the spleen.

Example 58: Direct Comparison of Single Dose Treatment with Anti-huCD52 in huCD52 Transgenic Mice

The depleting activity of several humanized anti-CD52 antibodies (2C3-SFD1/K12, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13, and 9D9-H18/K13) was compared in the huCD52 transgenic mouse. Mice were injected with antibodies i.v. at 1 mg/kg. At 2-hours post dosing, serum was collected for cytokine analysis. Three days later mice were sacrificed and blood and spleen collected to compare the level of lymphocyte depletion. Significant levels of B and T cell depletion were observed for all of the anti-CD52 antibodies (2C3-SFD1/K12, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13, and 9D9-H18/K13) and were comparable to those observed following Campath-1H® administration. Subset analysis also revealed no significant differences in the level of depletion for each antibody (2C3-SFD1/K12, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13, and 9D9-H18/K13) in either blood or spleen. Following injection of Campath-1H®, there was a marked increase in the circulating levels of both IL-6 and TNFα. Although injection of each of the anti-CD52 antibodies (2C3-SFD1/K12, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13, and 9D9-H18/K13) resulted in a significant decrease in the level of TNFα compared to Campath-1H®, the levels of IL-6 were similar.

FIGS. 86A-86E show the level of bulk lymphocyte populations (CD4+ T cells, CD8+ T cells, and B220+ B cells) and CD4+ T cell, CD8+ T cell, B220+B/NK cell, and myeloid cell subtypes in the blood 72 hours after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies. FIGS. 87A-87E show the level of bulk lymphocyte populations (CD4+ T cells, CD8+ T cells, and B220+ B cells) and CD4+ T cell, CD8+ T cell, B220+B/NK cell, and myeloid cell subtypes in the spleen 72 hours after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies. FIGS. 88A-88C show the levels of circulating cytokines 2 hours after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12, 12G6-SFD1/K11, 12G6-SFD1/K12, 9D9-H16/K13, and 9D9-H18/K13 antibodies.

Example 59: In Depth Depletion of Lymphocytes in huCD52 Transgenic Mice Following Single Dose Treatment with Anti-huCD52 Antibodies

Extensive depletion analysis was performed in the huCD52 transgenic mouse using anti-CD52 2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12 antibodies. Mice (N=4) were injected i.v. with a single dose of each antibody at 1 mg/kg. Three days later, the mice were sacrificed, and blood, spleen, lymph nodes, and thymus were collected to compare the level of lymphocyte depletion using multi-color flow cytometry analysis. Significant levels of B and T cell depletion were observed for all of the anti-CD52 2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12 antibodies and were comparable to those observed following Campath1H® administration in each tissue examined. Subset analysis also revealed no significant differences in the level of depletion for each antibody in either blood or spleen. Significant levels of lymphocyte depletion were also observed in the lymph nodes of mice. There did, however, appear to be some variability in the activity of the antibody, especially when looking at the central and effector memory T cell subset. Due to technical issues regarding the LSR-II and the CD8 stain, the thymus could not be evaluated.

FIGS. 89A-89D show the level of CD4+ T cell, CD8+ T cell, B220+ B cell, and NK/myeloid cell subtypes in the blood 72 hours after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12 antibodies. FIGS. 90A-90D show the level of CD4+ T cell, CD8+ T cell, B220+ B cell, and NK/myeloid cell subtypes in the spleen 72 hours after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12 antibodies. FIGS. 91A-91D show the level of CD4+ T cell, CD8+ T cell, B220+ B cell, and NK/myeloid cell subtypes in the lymph node 72 hours after dosing with Campath-1H® (“Campath”), 2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12 antibodies.

Example 60: Creation and Evaluation of the huCD52 Knock-in/Knock-Out (KI/K0) Transgenic Mouse on the C57BL/6 Background

A new human CD52 knock-in/knock-out mouse model was created on the C57Bl/6 background. To create this mouse, the mouse CD52 gene sequence was replaced by the human CD52 gene sequence. The targeting strategy allowed for the replacement of the mouse sequence with the human sequence while maintaining the exon-intron structure. A selection marker was used to identify progeny containing the new gene sequence. The final allele was created by removal of the selection marker leaving only the human CD52 gene sequence.

Basic characterization of the huCD52 KI/KO mouse model involved determining the level of human CD52 expression on lymphocytes. Blood from huCD52-KI/KO transgenic mice (N=4) and C57BL/6 mice (N=2) were stained for hCD52 expression and the number of CD52 molecules/cell was enumerated using the Bang's labs Simply Cellular anti-human antibody assay. Staining of peripheral blood cells from huCD52-KI/KO transgenic mice demonstrated that expression of huCD52 is very high on the majority of lymphocytes from these animals. Expression levels were similar to those observed in human CD4, CD8, and B cell populations. Expression levels on NK cells and macrophages were lower than those observed for T cells and B cells. An increased level of huCD52 expression was detected on neutrophils in these mice, contrary to the decreased expression level in human neutrophils or similar cells from the original transgenic mouse line on the CD-1 background. Similar levels of CD52 expression were observed on T and B cells from the original huCD52 CD1 transgenic mouse and the huCD52 KI/KI mouse.

FIG. 92A shows the huCD52 expression level on CD4+ T cell, CD8+ T cell, B220+ B cell, and NK/myeloid cell subtypes in huCD52-KI/KO and non-transgenic control mice. FIG. 92B shows the huCD52 expression level on CD4+ T cells, CD8+ T cells, and B cells in huCD52-KI/KO and huCD52 CD1 transgenic mice.

Example 61: Direct Comparison of Depletion Characteristics Between Small and Large Scale Lots of 12G6 and 2C3

huCD52 KI/KO transgenic mice were dosed with 12G6-SFD1/K12 or 2C3-SFD1/K12 to determine the depleting activity. In addition, activity was examined using antibodies generated from two different sources (small scale and large scale lots) at Genzyme. Mice were injected i.v. with each antibody at 1 mg/kg. Three days post injection, mice were sacrificed, and blood was collected for flow cytometry analysis to determine the levels of circulating CD4+ and CD8+ T cells, B cells, NK cells, neutrophils and macrophages. No significant differences in depletion of CD4 T cells, CD8+ T cells, B cells, and NK cells were observed between the small scale and large scale lot derived antibodies.

The various lots of 12G6-SFD1/K12 and 2C3-SFD1/K12 antibodies were also evaluated by flow cytometry to compare the intensity of staining on splenocytes from huCD52-KI/KO transgenic mice. Both 12G6-SFD1/K12 and 2C3-SFD1/K12 antibodies appear to recognize human CD52 to the same extent as Campath-1H® on isolated splenocytes. In addition, there was no difference in the level of recognition between the two sources (small scale and large scale lots) of antibody.

FIGS. 93A-93B show binding to huCD52 of 12G6-SFD1/K12 and 2C3-SFD1/K12 antibodies (from various production sources) as compared to a Campath-1H® control. FIG. 94 shows the level of bulk lymphocyte populations (CD4+ T cells, CD8+ T cells, and B220+ B cells) in the blood 72 hours after dosing with 12G6-SFD1/K12 and 2C3-SFD1/K12 antibodies from various production sources.

Example 62: Analysis of PK Profile for Anti-CD52 Antibodies in huCD52-KI/KO Transgenic Mice

The pharmacokinetic profiles of humanized 2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12 antibodies were determined in huCD52 KI/KO transgenic mice. Mice were injected i.v. with antibodies at 1 mg/kg, and blood was collected at various timepoints beginning two hours post dosing. The circulating levels of each antibody were evaluated using an anti-human Ig ELISA. The overall clearance rate was similar for each of the humanized anti-CD52 2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12 antibodies with 2C3-SFD1/K12 exhibiting potentially faster kinetics, while 12G6-SFD1/K12 was present in the serum for the longest period of time.

FIGS. 95A-95B show the levels of 2C3-SFD1/K12, 9D9-H16/K13 and 12G6-SFD1/K12 antibodies in the blood over a timecourse after dosing.

Example 63: Evaluation of 12G6 and 2C3 Pretreatment on EAE in huCD52-KI/KO Transgenic Mice

The efficacy of anti-CD52 antibody treatment on reducing the overall disease incidence and severity of Experimental Autoimmune Encephalomyelitis (EAE) was evaluated in huCD52 KI/KO mice. huCD52-KI/KO mice were treated with a course of either 2C3-SFD1/K12 or 12G6-SFD1/K12 on days −5 thru −1. EAE (a model of multiple sclerosis) was induced by immunization with MOG35-55 peptide emulsified in CFA, and treatment with pertussis toxin, on days 0 and 2. Vehicle treated mice began to display signs of paralysis by day 10 post injection, which developed into severe progressive disease. In contrast, pretreatment of mice with either the 2C3-SFD1/K12 or 12G6-SFD1/K12 antibody delayed the onset of disease and decreased the overall disease severity.

FIG. 96 demonstrates the EAE clinical score of 2C3-SFD1/K12 and 12G6-SFD1/K12 over a timecourse of disease progression.

Example 64: Fc Modification of Antibodies to Alter the Pharmacokinetic Profile of Anti-CD52 Antibodies

Alterations in the Fc region of antibodies 1) affect the biological activity of the antibody by altering interactions with Fc receptors and/or 2) alter the pharmacokinetic profile of the antibody by altering interactions with the FcRn neonatal receptor. The FcRn molecule is expressed on vascular endothelium and is believed to be the main site of IgG recycling. The FcRn binds to the antibody Fc portion which then becomes internalized within a cell. Antibodies that have high affinity interactions with the FcRn will be recycled back to the surface of the cell and will be released back into circulation. Antibodies that have lower affinity interactions dissociate within the cell and ultimately degrade. Site directed mutagenesis to increase the interaction with FcRn generates an antibody that can be maintained in circulation for longer periods of time compared to an unmodified antibody. Conversely, mutations within the Fc region of an antibody that decrease FcRn binding shorten the circulating half-life of the antibody. Mutations that have been described to decrease binding to FcRn resulting in shorter circulating half-lives include the His435Ala single mutation and the His310A1a/His435Gln double mutation (see, e.g., Kim et al., “Mapping the site on human IgG for binding of the MHC class I-related receptor, FcRn,” Eur. J. Immunol., 29:2819-2825 (1999) and Kenanova et al., “Tailoring the Pharmacokinetics and Positron Emission Tomography Imaging Properties of Anti-Carcinoembryonic Antigen Single-Chain Fv-Fc Antibody Fragments,” Cancer. Res. 65(2):622-631 (2005)).

The 2C3-SFD1/K12 antibody was mutated to generate His435Ala 2C3-SFD1/K12 (“2C3-SFD1/K12-Modified 1”) and His310A1a/His435Gln 2C3-SFD1/K12 (“2C3-SFD1/K12-Modified 2”) antibodies that have altered PK profiles. Biacore analysis was conducted to confirm decreased binding to both mouse and human FcRn molecules. Both Campath-1H® and 2C3-SFD1/K12 antibodies bound to each of the mouse and human FcRn molecules with similar kinetics. In contrast, His435Ala 2C3-SFD1/K12 antibodies bound at low levels to the mouse FcRn but not to human FcRn. His310A1a/His435Gln 2C3-SFD1/K12 antibodies did not bind to either mouse or human FcRn molecule, indicating that the incorporation of either the single or double mutation into the 2C3-SFD1/K12 Fc region significantly affects binding to mouse and human FcRn.

FIGS. 97A-97B demonstrate the ability of Campath1H® (“Campath”), 2C3-SFD1/K12 (“2C3”), His435Ala 2C3-SFD1/K12 (“H435A 2C3”) and His310A1a/His435Gln 2C3-SFD1/K12 (“H310A/H435Q 2C3”) to bind to mouse and human FcRn molecules.

Example 65: Evaluation of the Half-Life of Fc Modified Anti-CD52 Antibodies Following I.V. Administration in C57Bl/6 Mice

Fc modifications were incorporated into the 2C3-SFD1/K12 backbone to generate 2C3-SFD1/K12-Modified 1 and 2C3-SFD1/K12-Modified 2 antibodies that exhibited decreased binding to the FcRn receptor responsible for maintaining antibodies in circulation. The pharmacokinetic profile was determined for the 2C3-SFD1/K12 antibody and the 2C3-SFD1/K12-Modified 1 and 2C3-SFD1/K12-Modified 2 antibodies with reduced FcRn binding. C57BL/6 mice were used to evaluate the PK profile in the absence of target antigen (2C3-SFD1/K12 binds to human CD52 but does not cross-react with mouse CD52). Mice were injected i.v. with antibodies at 1 mg/kg. At various timepoints, blood was collected to analyze the level of circulating human IgG1 in the mouse serum by ELISA. Both 2C3-SFD1/K12-Modified 1 and 2C3-SFD1/K12-Modified 2 antibodies were cleared from the blood faster than the 2C3-SFD1/K12 antibody. 2C3-SFD1/K12 had a half-life of 403 hrs, while 2C3-SFD1/K12-Modified 1 had a half-life of 51 hours and 2C3-SFD1/K12-Modified 2 had a half-life of 8 hours. PK profiles for 2C3-SFD1/K12 and 2C3-SFD1/K12-Modified-1 were consistent with a 1-compartment model with only a single phase of elimination. In contrast, profiles for 2C3-SFD1/K12-Modified-2 were consistent with a 2 compartment model, with 2 distinct phases of elimination (specified as alpha and beta in the table). The first phase lasted until 48 hr post dose (alpha) and the second phase (beta, also called the terminal elimination phase) started 48 hr post dose.

FIG. 98 shows the in vivo clearance of 2C3-SFD1/K12 (“2C3 unmodified”), 2C3-SFD1/K12-Modified 1 (“2C3-Fc mutant 1”) and 2C3-SFD1/K12-Modified 2 (“2C3-Fc mutant 2”) in nontransgenic mice.

TABLE 17 Summary of Pharmacokinetic Data Across Groups 2C3-SFD1/K12- 2C3-SFD1/K12- 2C3-SFD1/K12 Modified 1 Modified 2 t_(1/2) (hr) 403 ± 140 51.0 ± 12.3 8.05 ± 0.74 (Alpha) 282 ± 385 (Beta) Cl (ml/hr/kg) 0.29 ± 0.09 1.35 ± 0.36 5.90 ± 4.67 Vz (ml/kg)  156 ± 40.7 94.8 ± 14.3 1932 ± 1341 AUC (ug*hr/ 3748 ± 937  781 ± 171 230 ± 105 ml) Cmax (ug/ml) 9.65 ± 1.72 11.9 ± 0.83 9.64 ± 3.70

TABLE 18 Individual Animal Data HL_Lambda_z Cmax AUCINF_obs Vz_obs Cl_obs Group^(#) Animal (hr) (ug/ml) (hr*ug/ml) (ml/kg) (ml/hr/kg) 2C3 2.1 197.26 11.56 2967.86 95.89 0.34 2C3 2.2 494.01 10.54 4635.96 153.73 0.22 2C3 2.3 324.61 10.06 3783.76 123.77 0.26 2C3 2.4 283.68 10.57 3130.92 130.72 0.32 2C3 2.5 330.89 6.15 2025.29 235.71 0.49 2C3 2.6 547.78 10.56 4469.73 176.81 0.22 2C3 2.7 597.92 10.57 4764.75 181.04 0.21 2C3 2.8 320.65 7.61 3415.82 135.43 0.29 2C3 2.9 527.01 9.27 4533.82 167.70 0.22 AVG 402.65 9.65 3747.55 155.64 0.29 SD 140.22 1.72 937.38 40.73 0.09 2C3-M1 3.1 35.20 12.84 513.50 98.89 1.95 2C3-M1 3.2 42.74 11.68 842.55 73.17 1.19 2C3-M1 3.3 50.55 11.39 902.62 80.80 1.11 2C3-M1 3.4 46.61 12.49 717.95 93.67 1.39 2C3-M1 3.5 56.38 12.94 911.32 89.26 1.10 2C3-M1 3.6 63.40 12.41 995.22 91.91 1.00 2C3-M1 3.7 33.86 12.02 513.17 95.19 1.95 2C3-M1 3.8 63.14 10.56 842.79 108.08 1.19 2C3-M1 3.9 66.75 11.02 788.59 122.12 1.27 AVG 50.96 11.93 780.86 94.79 1.35 SD 12.30 0.83 170.51 14.33 0.36 Alpha Beta HL_Lambda HL_Lambda Cmax AUCINF_obs Vz_obs Cl_obs Group^(#) Animal (hr) (hr) (ug/ml) (hr*ug/ml) (ml/kg) (ml/hr/kg) 2C3-M2 4.1* 8.31 Missing 10.62 177.07 67.74 5.65 2C3-M2 4.2 7.42 994.71 11.35 390.03 3679.37 2.56 2C3-M2 4.3 7.37 703.09 10.48 315.82 3211.80 3.17 2C3-M2 4.4 7.72 227.03 11.78 247.96 1320.92 4.03 2C3-M2 4.5** Missing Missing Missing Missing Missing Missing 2C3-M2 4.6** Missing Missing Missing Missing Missing Missing 2C3-M2 4.7*** 77.89 77.89 1.32 61.71 1820.87 16.20 2C3-M2 4.8 8.18 150.98 11.41 221.89 981.64 4.51 2C3-M2 4.9 9.33 77.61 10.49 194.31 576.21 5.15 AVG 8.05 281.98 9.64 229.83 1931.80 5.90 SD 0.74 384.82 3.70 104.69 1341.43 4.67 ^(#)-The tested groups were 2C3-SFD1/K12 (“2C3”), 2C3-SFD1/K12- Modified 1 (“2C3-M1”) and 2C3-SFD1/K12-Modified 2 (“2C3-M2”) *Animal 4.1 no beta t1/2, Vz outlier. **-Animals 4.5 & 4.6, not enough data for PK analysis. ***Animal 4.7 incomplete injection

Example 66: Evaluation of the Half-Life of Fc Modified Anti-CD52 Antibodies Following I.V. Administration in Heterozygous huCD52 Transgenic Mice

The pharmacokinetic profile was determined for the 2C3-SFD1/K12 antibody and the 2C3-SFD1/K12-Modified 1 and 2C3-SFD1/K12-Modified 2 antibodies with reduced FcRn binding in vitro. huCD52 transgenic mice were used to evaluate the PK profile in the presence of the 2C3-SFD1/K12 antibody target antigen. Mice were injected i.v. with antibodies at 1 mg/kg. At various timepoints, blood was collected to determine the level of circulating human IgG1 in the mouse serum by ELISA. Both 2C3-SFD1/K12-Modified 1 and 2C3-SFD1/K12-Modified 2 antibodies were cleared from the blood faster than the 2C3-SFD1/K12 antibody. 2C3-SFD1/K12 had a half-life of 64 hrs, while 2C3-SFD1/K12-Modified 1 had a half-life of 32 hours, and 2C3-SFD1/K12-Modified 2 had a half-life of 6.5 hours.

FIG. 99 shows the in vivo clearance of 2C3-SFD1/K12 (“2C3”), 2C3-SFD1/K12 modified 1 (“2C3-Fc mutant 1”) and 2C3-SFD1/K12 modified 2 (“2C3-Fc mutant 2”) in huCD52 transgenic mice.

TABLE 19 Summary of Pharmacokinetic Data Across Groups 2C3-SFD1/ 2C3-SFD1/K12- 2C3-SFD1/K12- K12 Modified 1 Modified 2 t_(1/2) (hr) 64.2 ± 12.1 32.3 ± 3.25 6.58 ± 2.03 Cl (ml/hr/kg) 2.15 ± 0.31 2.51 ± 0.28 5.41 ± 0.83 Vz (ml/kg)  198 ± 42.8  117 ± 21.1 49.7 ± 11.1 AUC (ug*hr/ml)  475 ± 73.4  403 ± 44.5  188 ± 27.2 Cmax (ug/ml) 8.88 ± 1.69 12.4 ± 1.67 12.9 ± 1.91

TABLE 20 Individual Animal Data HL_Lambda_z Cmax AUCINF_obs Vz_obs Cl_obs Group# Animal (hr) (ug/ml) (hr*ug/ml) (ml/kg) (ml/hr/kg) 2C3 2.1 77.32 8.19 421.87 264.42 2.37 2C3 2.11 61.47 10.38 483.25 183.51 2.07 2C3 2.2 78.28 9.28 496.58 227.42 2.01 2C3 2.3 82.38 6.99 441.98 268.91 2.26 2C3 2.4 53.60 9.08 465.09 166.28 2.15 2C3 2.5 58.02 9.09 526.59 158.95 1.90 2C3 2.6 44.97 6.03 371.17 174.78 2.69 2C3 2.7 56.52 9.38 476.41 171.16 2.10 2C3 2.8 67.99 12.13 641.28 152.97 1.56 2C3 2.9 61.46 8.30 421.65 210.29 2.37 Mean 64.20 8.88 474.59 197.87 2.15 SD 12.06 1.69 73.40 42.80 0.31 2C3-M1 3.1 28.48 15.19 412.41 99.64 2.42 2C3-M1 3.11 34.64 12.60 468.36 106.69 2.14 2C3-M1 3.2 27.57 14.17 411.82 96.60 2.43 2C3-M1 3.3 34.27 11.96 401.38 123.20 2.49 2C3-M1 3.4 29.10 12.51 400.36 104.85 2.50 2C3-M1 3.5 29.63 11.11 470.98 90.77 2.12 2C3-M1 3.6 32.76 9.75 348.72 135.53 2.87 2C3-M1 3.7 35.68 10.41 328.71 156.61 3.04 2C3-M1 3.8 36.41 13.52 390.24 134.61 2.56 2C3-M1 3.9 34.06 12.39 392.53 125.19 2.55 Mean 32.26 12.36 402.55 117.37 2.51 SD 3.25 1.67 44.48 21.05 0.28 2C3-M2 4.1 7.64 13.45 197.24 55.85 5.07 2C3-M2 4.11 Missing 9.00 Missing Missing Missing 2C3-M2 4.2 7.79 14.92 217.80 51.61 4.59 2C3-M2 4.3 7.35 12.79 183.44 57.78 5.45 2C3-M2 4.4 3.54 10.34 152.92 33.44 6.54 2C3-M2 4.5 Missing Missing Missing Missing Missing 2C3-M2 4.6 Missing Missing Missing Missing Missing 2C3-M2 4.7 Missing Missing Missing Missing Missing 2C3-M2 4.8 Missing Missing Missing Missing Missing 2C3-M2 4.9 Missing Missing Missing Missing Missing Mean 6.58 12.10 187.85 49.67 5.41 SD 2.03 2.40 27.23 11.12 0.83 PK parameters not available for 4.11, 4.5, 4.6, 4.7, 4.8, and 4.9 due to insufficient data. #-The tested groups were 2C3-SFD1/K12 (“2C3”), 2C3-SFD1/K12-Modified 1 (“2C3M1”) and 2C3-SFD1/K12-Modified 2 (“2C3-M2”)

Example 67: Evaluation of In Vivo Depletion Following I.V. Administration of Fc Modified Anti-CD52 Antibodies in Heterozygous huCD52 Transgenic Mice

The depletion activity was determined for the 2C3-SFD1/K12, 2C3-SFD1/K12-Modified 1, and 2C3-SFD1/K12-Modified 2 antibodies in huCD52 transgenic mice. Mice were treated with 1 mg/kg of 2C3-SFD1/K12, 2C3-SFD1/K12-Modified 1, or 2C3-SFD1/K12-Modified 2 antibodies and evaluated for the presence of CD4 T cells, CD8+ T cells, B cells, and NK cells 72 hours later. Administration of 2C3-SFD1/K12-Modified 1 or 2C3-SFD1/K12-Modified 2 antibodies resulted in decreased levels of depletion in the blood and spleen compared administration of 2C3-SFD1/K12 antibodies. Further, 2C3-SFD1/K12-Modified 1 elicited greater depletion than 2C3-SFD1/K12-Modified 2 in both the blood and spleen

FIGS. 100A-100B show the level of bulk lymphocyte populations (CD4+ T cells, CD8+ T cells, B220+ B cells, and NK cells) in the blood and spleen 72 hours after dosing with 2C3-SFD1/K12 (“2C3”), 2C3-SFD1/K12 modified 1 (“2C3 Fc mutant-1”), and 2C3-SFD1/K12 modified 2 (“2C3 Fc mutant-2”) antibodies.

Example 68: Detailed Epitope Specificities of Humanized Anti-CD52 Antibodies

Detailed epitope specificities of the humanized 12G6-SFD1/K12, 2C3-SFD1/K12, and 9D9-H16/K13 antibodies were determined using a Biacore T100 instrument. As a control, the epitope specificity of clone 097 (purified anti-human CD52 antibody, Biolegend) was evaluated using the same methodologies. The epitope specificity of clone 097 had previously been characterized using a peptide ELISA method (Hale G, “Synthetic peptide mimotype of the CAMPATH-1 (CD52) antigen, a small glycosylphosphatidylinositol-anchored glycoprotein,” Immunotechnology, 1:175-187 (1995)). In this Biacore T100 assay, the antibodies were directly immobilized on Biacore CMS Series S carboxymethyl dextran sensor chips (GE # BR-1006-68) using amine coupling. The carboxymethyl dextran surface was activated using a 1:1 mixture of 0.1M N-hydroxysuccinimide (NHS) and 0.4M N-ethyl-N′-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC), allowing the surface to bind reactive amine groups on the antibodies. Because IgM antibodies tend to have a higher level of non-specific binding compared to IgGs, the binding of a mouse IgMκ (mIgMκ) isotype control (Biolegend clone # MM-30) was also investigated. Following antibody immobilization, the reactive sensor chip surface was quenched using 1M ethanolamine hydrochloride/NaOH pH 8.5. One flow cell on each chip was a blank reference surface, and subsequent flow cells were immobilized with 10,000 RU of antibody.

A series of alanine-scanning mutant peptides comprising the human CD52 sequence (MUT 1-MUT 12 (SEQ ID NOS: 169-180, respectively), Table 21) (see, e.g., Hale G, “Synthetic peptide mimotype of the CAMPATH-1 (CD52) antigen, a small glycosylphosphatidylinositol-anchored glycoprotein,” Immunotechnology, 1:175-187 (1995)) were synthesized. Antibody binding to these mutant CD52 peptides and to wildtype human CD52 peptides was tested at concentrations of 500 nM, 100 nM, 50 nM, and 0 nM. Peptides were diluted into the assay running buffer, HBS-EP+ (10 mM HEPES, 150 mM NaCl, 0.05% P20 surfactant, 3 mM EDTA, pH 7.4). Duplicates of 100 nM samples were included. The light (kappa) chain specific rat anti-mouse IgM antibody (Southern Biotech Clone #1B4B1) was also included as an IgM control. The T100 instrument sample chamber and assay temperatures were set to 4° C. and 25° C., respectively. The human CD52 peptide samples were injected for five minutes at a 50 μl/min flow rate to measure association, and washed in HBS-EP+ for five minutes at a 50 μl/min flow rate to measure dissociation. The antibody surface was stripped of any remaining bound peptide using a sixty second injection of 10 mM glycine-HCl pH 2.0 at a 50 μl/min flow rate. Analysis was performed using Biacore T100 Kinetics Evaluation software v2.0 (GE Healthcare). Data was fit to a 1:1 model with reference flow cell and 0 nM concentration subtraction (double-reference subtraction). Representative sensorgrams of 12G6-SFD1/K12 antibody negative ((−), MUT 8) and positive ((+), MUT 9) peptide epitope recognition are shown in FIG. 101A and FIG. 101B, respectively. The compiled peptide binding data is summarized in Table 21.

The previously characterized binding specificity of clone 097 (Hale G, “Synthetic peptide mimotype of the CAMPATH-1 (CD52) antigen, a small glycosylphosphatidylinositol-anchored glycoprotein,” Immunotechnology, 1:175-187 (1995)) was determined by coating ELISA plates with peptides containing the six residues of the C-terminal portion of human CD52 and then measuring the binding of the antibody to the fixed peptide. Each of the residues was substituted by all 20 amino acids. Because the peptides were attached to a solid surface in this ELISA, the assay may have been more influenced by avidity effects than the Biacore T100 assay described herein, which uses an antibody fixed to the surface over which the peptides are flowed. In the ELISA study, alanine substitutions at positions 11 and 12 (wildtype residues proline and serine, respectively) of the mature form of human CD52 were found to reduce strong binding of clone 097 to the peptide. In the present Biacore T100 study, alanine substitutions at positions 11 and 12 (as well as positions 7, 8, 9, and 10) were found to abrogate binding of clone 097. The hypothesized avidity effects of the ELISA assay are likely the reason why the mapped epitope of clone 097 is smaller as determined by the ELISA method than as determined by the described Biacore T100 assay.

The binding of both the 2C3-SFD1/K12 and 12G6-SFD1/K12 humanized antibodies to the human CD52 peptide sequence is sensitive to alanine substitutions at positions 7, 8, and 11 and the binding of humanized 9D9-H16/K13 is sensitive to alanine substitutions at positions 4 and 11. These defined epitope specificities overlap with the results observed in Example 4 (summarized in Table 8). Slight variations between the results are not unexpected given that the Biacore T100 method used to measure binding in the present case was significantly different from the method used in Example 4. In contrast to the present case, in Example 4, engineered CHO cells were used to express wildtype or alanine-substituted mutants of human CD52. Human CD52 expressed in such mammalian cells can be glycosylated, affecting binding. This is not the case for the human CD52 used in the Biacore T100 assay.

TABLE 21 Binding to alanine-scanning mutant hCD52 peptides SEQ 2C3- 9D9- 12G6- Control ID Peptide SFD1/K12 H16/K13 SFD1/K12 097 mIgM Peptide NO: Sequence Binding Binding Binding Binding Binding MUT 1 169 A QNDTSQTSSPSADC + + + + - MUT 2 170 G A NDTSQTSSPSADC + + + + - MUT 3 171 GQ A DTSQTSSPSADC + + + + - MUT 4 172 GQN A TSQTSSPSADC + - + + - MUT 5 173 GQND A SQTSSPSADC + + + + - MUT 6 174 GQNDT A QTSSPSADC + + + + - MUT 7 175 GQNDTS A TSSPSADC - + - - - MUT 8 176 GQNDTSQ A SSPSADC - + - - - MUT 9 177 GQNDTSQT A SPSADC + + + - - MUT 10 178 GQNDTSQTS A PSADC + + + - - MUT 11 179 GQNDTSQTSS A SADC - - - - - MUT 12 180 GQNDTSQTSSP A ADC + + + - - Controls WT 1 181 GQNDTSQTSSPSADK- + + + + - Biotin WT 2 182 Biotin- + - + + - GQNDTSQTSSPSAD Rat anti- N/A N/A N/A N/A N/A + + mIgM (+)Binding detected: Maximum response (R_(max)) >2RUs for 500 nM peptide injection (-)No binding detected: Maximum response (R_(max)) <2RUs for 500 nM peptide injection

Example 69: Assessment of CD4+ T Cell Responses Induced by Campath-1H® or 12G6-SFD1/K12

The CD4+ T cell proliferative response was evaluated after repeated in vitro stimulation with autologous dendritic cells (DC) preloaded with a set of overlapping 15-mer peptides comprising sequences from the variable regions of either Campath-1H® or the humanized 12G6-SFD1/K12 antibody. These experiments utilized normal human donor T cells and DCs. Results were measured by quantifying tritiated thymidine incorporation of the proliferating human CD4+ T cells in response to autologous peptide pulsed antigen presenting cells (APC).

Cell preparation: PBMCs were isolated from a normal human donor apheresis product acquired from BioMed Supplies (Carlsbad, Calif.). HLA haplotype screening of the donor blood was performed by Key Biologics, LLC (Memphis, Tenn.) (Table 22). PBMCs were isolated using the Ficoll-Paque PLUS density gradient (GE Healthcare) and a series of washes with phosphate buffered saline (PBS, Invitrogen, Carlsbad, Calif.). CD4+ T cells were isolated from PBMC using the Dynal CD4+ bead-based positive isolation kit (Invitrogen), following the manufacturer's recommended protocol. Isolated CD4+ T cells were frozen in Recovery Cell Culture Freezing Media (Invitrogen) and stored in liquid nitrogen. Dendritic Cells (DC) were induced from PBMCs by plating adherent cells with GM-CSF (Leukine, Bayer, Leverkusin, Germany) and IL-4 (Peprotech, Rocky Hill, N.J.) for six days. Media supplemented with GM-CSF and IL-4 was replaced on day 4. DCs were subsequently isolated from the flasks and frozen in the Freezing Media then transferred to liquid nitrogen storage tanks.

TABLE 22 HLA haplotype of blood donors Donor HLA DR haploytpe peptide set BMS170 DRB1_0701 DRB1_1503 Campath BMS154 DRB1_0301 DRB1_0302 Campath BMS150 DRB1_1101 DRB1_1302 Campath BMS167 DRB1_0701 DRB1_1503 Campath BMS200 DRB1_0804 DRB1_1202 Campath BMS301 DRB1_1401 DRB1_1503 Campath BMS352 DRB1_0301 DRB1_1101 Campath BMS362 DRB1_0302 DRB1_0302 Campath BMS484 DRB1_0103 DRB1_1201 Campath/GLD52 BMS486 DRB1_1302 DRB1_1303 Campath/GLD52 BMS640 DRB1_0301 DRB1_1302 GLD52 BMS656 DRB1_301 DRB1_1101 GLD52 BMS902 DRB1_0302 DRB1_0804 GLD52 BMS928 DRB1_1001 DRB1_1503 GLD52 BMS927 DRB1_1001 DRB1_1503 GLD52 BMS963 DRB1_0302 DRB1_1401 GLD52 BMS361 DRB1_1102 DRB1_1401 GLD52 BMS165 DRB1_1102 DRB1_1501 GLD52

Peptide: Peptides encompassing the heavy and light chain variable regions of Campath-1H® and 12G6-SFD1/K12 were synthesized using a Rainin Symphony automated peptide synthesizer using standard Fmoc-chemistry on CLEAR resin (Peptides International, Louisville, Ky.). Amino acids (EMD Biosciences, San Diego, Calif. or Anaspec, San Jose, Ca) were orthogonally protected with tert-Butoxycarbonyl (BOC), tert-Butyl (tBu), 2,2,4,6,7-Pentamethyldihydro-benzofuran-5-sulfonyl (Pbf), or Trityl (Trt) groups. Couplings were performed using an amino acid/HCTU/HOBt/DIEA/resin with a molar ratio of 6:6:3:12:1. A solution of 20% Piperidine and 2.5% 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in DMF was used to remove Fmoc from the amino terminus during each cycle. Deprotection/cleavage from resin was performed using a cocktail of 15 mls/0.1 mM resin of 2.5% water/2.5% TIS/5% Anisole/90% TFA v/v ratio for 3 hours. Supernatant was precipitated in diethyl-ether (−80° C.) and pelleted at 3000 rpm for 10 minutes. Ether was decanted and the pellet was washed again. Crude peptide was then lyophilized. Analytical HPLC (XBridge C18 4.5×100 mm, Waters Corp., Milford, Mass.) and MALDI-TOF mass spectrometry (Synapt, Waters Corp., Milford, Mass.) were used to verify the sequences and assess purity. All reagents were HPLC grade (EMD Biosciences, San Diego, Ca or Sigma Aldrich, St. Louis, Mo.). Lyophilized peptides were resuspended in 100% DMSO (Sigma). Forty three Campath-1H® peptides were combined into 11 linear groups, each containing 3 or 4 peptides per group (Table 23: from top to bottom, light chain peptides are denoted by SEQ ID NOs: 187-206 and heavy chain peptides are denoted by SEQ ID NOs: 207-229). The 42 12G6-SFD1/K12 peptides were combined into 8 linear groups, each containing five or six peptides per group (Table24: from top to bottom, light chain peptides are denoted by SEQ ID NOs: 230-250 and heavy chain peptides are denoted by SEQ ID NOs: 251-271).

TABLE 23 43 Campath-1H ® 15-mer light chain and heavy chain peptides, overlapping by 10 amino acids each Campath-1H ® Peptides light chain heavy chain Peptide ID# Peptide ID# DIQMTQSPSSLSASV 978 QVQLQESGPGLVRPS  998 QSPSSLSASVGDRVT 979 ESGPGLVRPSQTLSL  999 LSASVGDRVTITCKA 980 LVRPSQTLSLTCTVS 1000 GDRVTITCKASQNID 981 QTLSLTCTVSGFTFT 1001 ITCKASQNIDKYLNW 982 TCTVSGFTFTDFYMN 1002 SQNIDKYLNWYQQKP 983 GFTFTDFYMNWVRQP 1003 KYLNWYQQKPGKAPK 984 DFYMNWVRQPPGRGL 1004 YQQKPGKAPKLLIYN 985 WVRQPPGRGLEWIGF 1005 GKAPKLLIYNTNNLQ 986 PGRGLEWIGFIRDKA 1006 LLIYNTNNLQTGVPS 987 EWIGFIRDKAKGYTT 1007 TNNLQTGVPSRFSGS 988 IRDKAKGYTTEYNPS 1008 TGVPSRFSGSGSGTD 989 KGYTTEYNPSVKGRV 1009 RFSGSGSGTDFTFTI 990 EYNPSVKGRVTMLVD 1010 GSGTDFTFTISSLQP 991 VKGRVTMLVDTSKNQ 1011 FTFTISSLQPEDIAT 992 TMLVDTSKNQFSLRL 1012 SSLQPEDIATYYCLQ 993 TSKNQFSLRLSSVTA 1013 EDIATYYCLQHISRP 994 FSLRLSSVTAADTAV 1014 YYCLQHISRPRTFGQ 995 SSVTAADTAVYYCAR 1015 HISRPRTFGQGTKVE 996 ADTAVYYCAREGHTA 1016 RTFGQGTKVEIKRTV 997 YYCAREGHTAAPFDY 1017 EGHTAAPFDYWGQGS 1018 APFDYWGQGSLVTVS 1019 WGQGSLVTVSSASTK 1020

TABLE 24 42 12G6-SFD1/K12 15-mer light chain and heavy chain peptides, overlapping by 10 amino acids each 12G6-SFD1/K12 Peptides light chain heavy chain Peptide ID# Peptide ID# DIVMTQTPLSLSVTP 1027 EVQLVESGGGLVQPG 1048 QTPLSLVTPGQPAS 1028 ESGGGLVQPGGSLRL 1049 LSVTPGQPASISCKS 1029 LVQPGGSLRLSCAAS 1050 GQPASISCKSSQSLL 1030 GSLRLSCAASGFPFS 1079 ISCKSSQSLLYSNGK 1031 SCAASGFPFSNYWMN 1080 SQSLLYSNGKTYLNW 1032 GFPFSNYWMNWVRQA 1081 YSNGKTYLNWVLQKP 1072 NYWMNWVRQAPGKGL 1082 TYLNWVLQKPGQSPQ 1073 WVRQAPGKGLEWVGQ 1055 VLQKPGQSPQRLIYL 1074 PGKGLEWVGQIRLKS 1056 GQSPQRLIYLVSKLD 1036 EWVGQIRLKSNNYAT 1060 RLIYLVSKLDSGVPD 1037 IRLKSNNYATHYAES 1061 VSKLDSGVPDRFSGS 1038 NNYATHYAESVKGRF 1062 SGVPDRFSGSGSGTD 1039 HYAESVKGRFTISRD 1063 RFSGSGSGTDFTLKI 1040 VKGRFTISRDDSKNS 1064 GSGTDFTLKISRVEA 1041 TISRDDSKNSLYLQM 1065 FTLKISRVEAEDVGV 1042 DSKNSLYLQMNSLKT 1066 SRVEAEDVGVYYCVQ 1043 LYLQMNSLKTEDTAV 1067 EDVGVYYCVQGSHFH 1075 NSLKTEDTAVYYCTP 1068 YYCVQGSHFHTFGQG 1076 EDTAVYYCTPIDYWG 1083 GSHFHTFGQGTKLEI 1077 YYCTPIDYWGQGTTV 1084 TFGQGTKLEIKRTVA 1078 IDYWGQGTTVTVSSA 1085

In Vitro Stimulation

DC antigen pulsing and maturation: Before treatment with the peptides, DCs were thawed, washed and plated in RPMI (Invitrogen, Carlsbad, Calif.) supplemented with 5% Human Serum (HS, Sigma, St. Louis, Mo.), 1% Penicillin-Streptomycin (Invitrogen, Carlsbad, Calif.), 100 ng/ml GM-CSF, and 20 ng/ml IL-4. DCs were plated at 2×10⁵ cells/ml in 4 ml media in 6-well tissue culture plates and allowed to adhere for 1 hour at 37° C. Following cell adherence, 10 μg/ml (40 μg total) of each peptide were added to wells containing DCs, correlating to either 120 μg or 160 μg of total peptides added to each well (Campath-1H® 3-peptide or 4-peptide groups), or 200 μg or 240 μg of total peptide added to each well (12G6-SFD1/K12 5-peptide or 6-peptide groups). 40 μg of the pan-DR binding epitope (PADRE) were added to one well of DCs and served as a positive control, as it can bind to most HLA-DR molecules (Alexander J, et al., “Development of high potency universal DR-restricted helper epitopes by modification of high affinity DR-blocking peptides,” Immunity, 1:751-761 (1994)). Likewise, 40 μg of each of three HLA-DR binding Tetanus toxoid peptides (DTIMMEPPYCKGLDIYYKA (SEQ ID NO: 183), SAMLTNLIIFGPGPVLNKNEV (SEQ ID NO: 184), and NNFTVSFWLRVPKVSASHLE (SEQ ID NO: 185)) were added to one well of DCs. Similarly, a heat inactivated adenovirus was employed as a positive antigen source and was added to one well of DCs at 1 μg/ml. Lastly, one group of DCs remained unpulsed with antigen and served as a ‘null’ educated group. The DCs pulsed with the various antigens were incubated for at least three hours at 37° C. DCs were then treated with a ‘maturating cytokine cocktail’ containing 50 ng/ml TNF-α, 10 ng/ml IL-6, 25 ng/ml IL-1beta (Peprotech, Rocky Hill, N.J.) and 500 ng/ml PGE-2 (Sigma Aldrich, St. Louis, Mo.). The antigen pulsed DCs were then allowed to mature overnight at 37° C.

Establishment of co-culture: Following peptide loading and maturation, DCs were washed twice with PBS and replenished with 4 ml RPMI supplemented with 10% HS. Autologous CD4+ T cells were thawed and resuspended at 2×10⁶ cells/ml in RPMI supplemented with 10% HS, Penicillin, and Streptomycin. The DCs were then cultured with naïve CD4+ T cells at a 10:1 T cell:DC ratio (8×10⁶ T cells:8×10⁵ DCs) in 8 mls media. The co-culture was then incubated at 37° C. for 7 days. Approximately 72 hours after initiation of co-culture, the cells were supplemented with 25 IU recombinant IL-2 (Peprotech, Rocky Hill, N.J.), and further supplemented with 25 IU recombinant IL-2 in fresh media every 3-4 days thereafter.

Restimulation of co-culture: At day 7 (Stim #2) and day 14 (Stim #3), the co-cultures were restimulated following the above procedure.

Proliferation assay: DCs were plated, antigen pulsed and matured as stated above at 5×10⁵ cells/ml in 1 ml media on 24-well low binding plates to ease the subsequent transfer of cells to U-bottom assay plates. An irrelevant HLA DR binding peptide, CS 378-398 (peptide sequence DIEKKIAKMEKASSVFNVVNS (SEQ ID NO: 186)), was used as a negative control (Alexander J, et al., “Development of high potency universal DR-restricted helper epitopes by modification of high affinity DR-blocking peptides,” Immunity, 1:7 51-7 61 (1994)). Following 24 hour DC maturation, the cells were detached from plates using ice cold PBS washes. DCs were plated in U-bottom 96 well plates with the antigen stimulated T cells at a 1:1 T cell:DC ratio (2.5×10⁴ DC/well). Each T cell group was assayed in triplicate with DC pulsed with the educating peptide(s) (specific response) and DC pulsed with irrelevant peptide (nonspecific response), as well as T cell only and DC only controls. The assay proceeded for 72 hours prior to the addition of 1 uCi tritiated thymidine per well (Perkin Elmer, Waltham, Mass.). Cells were harvested on a 96 well plate harvester (Perkin Elmer) and the amount of tritiated thymidine incorporated quantified by measuring CPM on a Wallac Microbeta Trilux counter (Perkin Elmer). The stimulation index was calculated by dividing the specific CPM by the nonspecific CPM.

T Cell Receptor (TCR) V beta usage: Any CD4+ T cells remaining after establishment of the proliferation assay were frozen for eventual determination of T cell receptor V beta chain expression. Cells were thawed and stained with antibodies recognizing 24 conjugated Vbeta family members for 30 minutes following manufacturer's directions in the IOTest Beta Mark Kit (Beckman Coulter, France). After washing with PBS and resuspending in 1% formaldehyde, cells were analyzed on FACScalibur (Becton Dickinson, Franklin Lakes, N.J.). The percentage of cells expressing each of the detected V-beta chains was calculated, as summarized in FIG. 102 and FIG. 103.

Campath-1H® Immunogenicity Assessment

Immunogenicity assessment of Campath-1H® peptides was performed as described above using PBMCs from ten normal donors, from BioMedSupply (BMS). The summary of the responses as indicated by the stimulation index are depicted in Table 25A. Each donor is listed on one column, and each row lists the group of peptides used to stimulate CD4+ T cells. The Stimulation index (SI) is determined by dividing the specific immune response to the educating peptide group by an irrelevant response. SI values<2.0 are not listed. The proliferation data for each of the ten donors summarized in Table 25A is reported in FIG. 104A-J. Six donors exhibited a stimulation index greater than 2.0, and as a result were termed ‘Campath-1H® responders’. Educated CD4+ T cells from one of the responders, BMS352, exhibited specific immune responses when assayed with two different peptide groups. A seventh donor, BMS486, was also classified as ‘responder’. In this donor, a stimulation index 1.7 times background was recorded with the light chain peptide group 986-989. When assessing the V beta upregulation in the educated T cell cultures within this donor, it was shown that the 986-989 educated T cells exhibited high upregulation of a single V beta, V133 (FIG. 102). The upregulation of a single V beta and specific proliferative response indicated that BMS486 was a Campath-1H® responder. The three non-responding donors, BMS200, BMS154, and BMS167, did not show proliferative data or V beta upregulation, indicating that a peptide specific immune response did not occur. The Campath-1H® data was quantified as a 70% (7/10) responder rate. The total number of peptide groups eliciting an immune response was eight. Three of those eight immunogenic peptide groups elicited strong responses in the respective donors with stimulation indices of 3.0 or above (Table 26).

Table 25: Summary of Stimulation Index Data

TABLE 25A Campath-1H ® Stimulation Index BMS200 BMS301 BMS154 BMS484 BMS362 BMS486 BMS150 BMS167 BMS170 BMS352 982, 983, 984 & 987 nd 988, 989 & 990 985, 986, 991 & 992 2.6 993, 994, 995 & 996 997, 998 & 999 978, 979, 980, 981 982, 983, 984, 985 2.0 986, 987, 988, 989 2.1 1.7 990, 991, 992, 993 994, 995, 996, 997 2.1 998, 999, 1000, 1001 1002, 1003, 1004, 1005 1006, 1007, 1008, 1009 4.2 5.4 1010, 1011, 1012, 1013 3.0 1014, 1015, 1016, 1017 1018, 1019, 1020 PADRE 2.0 2.0 2.5 2.5 2.8 10.5 2.6 Tetanus 11.2 2.3 4.5 2.3 25.9 Ad-Bgal-HI 27.6 4.5 2.6 3.1 13.0 3.8 24.2 44.5 46.6 3.2 Null

TABLE 25B 12G6-SFD1/K12 Stimulation Index BMS484 BMS486 BMS656 BMS640 BMS361 BMS165 BMS902 BMS928 BMS927 BMS963 1027, 1028, 1029, 1030, 1031 1032, 1072, 1073, 1074, 1036 2.1 2.5 1037, 1038, 1039, 1040, 1041 1042, 1043, 1075, 1076, 1077, 1078 1048, 1049, 1050, 1079, 1080 1081, 1082, 1055, 1056, 1060 2.1 1061, 1062, 1063, 1064, 1065 2.0 nd 1066, 1067, 1068, 1083, 2.0 1084, 1085 PADRE 3.0 3.6 2.2 9.8 2.4 2.3 4.7 TT-974, 975, 976 2.9 5.2 3.2 5.7 12.9 3.7 4.3 22.4 Ad-Bgal 17.6 11.0 10.9 31.7 29.1 29.3 10.3 8.4 6.3 Null

Example 70: Assessment of CD4+ T Cell Responses Induced by 12G6-SFD1/K12

Immunogenicity assessment and V beta analysis of the variable region of 12G6-SFD1/K12 were performed as described in Example 69 for Campath-1H®, employing cells from ten normal donors. The proliferation data for each of the ten donors summarized in Table 25B is reported in FIG. 105A-J. Two of these ten donors were also used in the Campath-1H® assessment described above (BMS486 and BMS484), while the remaining eight donors were tested only with the 12G6-SFD1/K12 peptides. One donor, BMS484, responded to three peptide groups and was classified as a ‘12G6-SFD1/K12 responder’ (Table 25B). Two donors, BMS927 and BMS928, each responded to one group of peptides and were therefore also classified as responders. Donor BMS928 showed a weak stimulation index of 2.0 to the group containing heavy chain peptides 1066, 1067, 1068, 1083, 1084, and 1085. This response was confirmed by analyzing the proliferative T cells for V beta usage. The responding BMS928 T cells exhibited an upregulation of a single V beta, Vβ20 (FIG. 103). Donor BMS927 showed a stimulation index of 2.5 in T cells educated with one group of light chain peptides. V beta analysis of the responding BMS927 T cells did not indicate a single V beta upregulation over background. However, this donor remains in the ‘responder’ category, as the V beta kit represents only 70% of all possible V beta usages. The 12G6-SFD1/K12 rate of immunogenicity in these 10 donors was 30% (3/10), less than half the rate of Campath-1H® responders (70%). A total of five peptide groups elicited a response, while none of those five groups resulted in a stimulation index greater than 3.0 (Table 26).

TABLE 26 Summary of Campath-1H ® and 12G6-SFD1/K12 immune responses 12G6- Campath-1H ® SFD1/K12 Percentage of responders 70% (7/10) 30% (3/10) Number of peptide groups eliciting 8 5 response Responding peptide groups with 3/8 (38%) 0/3 (0%) Stimulation Index ≥ 3.0

SUMMARY

Peptides correlating to the heavy and light chain variable regions of humanized anti-CD52 monoclonal antibody 12G6-SFD1/K12 induced fewer immune responses from ten donors (30%) than peptides from the heavy and light chain variable regions of Campath-1H® (70%). The CD4+ T cell based immune responses that were generated with 12G6-SFD1/K12 were also of less magnitude than the Campath-1H® induced responses.

The following table lists the sequence identification numbers used herein.

TABLE 26 List of SEQ ID NOs SEQ ID NO TYPE DESCRIPTION   1 light chain variable Campath-1G ®   2 region (VL) CF1D12   3 8G3 (mouse)   4 4G7 (mouse)   5 9D9 (mouse)   6 11C11 (mouse)   7 3G7 (mouse)   8 5F7 (mouse)   9 12G (mouse)  10 23E6 (mouse)  11 2C3 (mouse)  12 7F11 (mouse)  13 4B10 (mouse)  14 heavy chain variable Campath-1G ®  15 region (VH) CF1D12  16 8G3 (mouse)  17 4G7 (mouse)  18 9D9 (mouse)  19 11C11 (mouse)  20 3G7 (mouse)  21 5F7 (mouse)  22 12G6 (mouse)  23 23E6 (mouse)  24 2C3 (mouse)  25 7F11 (mouse)  26 4B10 (mouse)  27 light chain CDR-1 Campath-1H ®  28 CF1D12 (mouse)  29 8G3, 4G7, 9D9, 11C11, 3G7 (mouse)  30 5F7 (mouse)  31 12G6, 23E6, 2C3 (mouse)  32 7F11 (mouse)  33 4B10 (mouse)  34 light chain CDR-2 Campath-1H ®  35 CF1D12 (mouse)  36 8G3, 11C11, 12G6, 23E6, 2C3 (mouse)  37 4G7 (mouse)  38 9D9 (mouse)  39 3G7 (mouse)  40 5F7 (mouse)  41 7F11, 4B10 (mouse)  42 light chain CDR-3 Campath-1H ®  43 CF1D12, 8G3, 4G7, 9D9, 11C11, 3G7, 5F7 (mouse)  44 12G6 (mouse)  45 23E6 (mouse)  46 2C3 (mouse)  47 7F11 (mouse)  48 4B10 (mouse)  49 heavy chain CDR-1 Campath-1H ®  50 CF1D12, 4G7, 9D9, 11C11, 3G7 (mouse)  51 8G3 (mouse)  52 5F7 (mouse)  53 12G6 (mouse)  54 23E6 (mouse)  55 2C3 (mouse)  56 7F11, 4B10 (mouse)  57 heavy chain CDR-2 Campath-1H ®  58 CF1D12 (mouse)  59 8G3 (mouse)  60 4G7 (mouse)  61 9D9, 11C11, 5F7 (mouse)  62 3G7 (mouse)  63 12G6, 2C3 (mouse)  64 23E6 (mouse)  65 7F11 (mouse)  66 4B10 (mouse)  67 heavy chain CDR-3 Campath-1H ®  68 CF1D12, 9D9 (mouse)  69 8G3, 4G7, 11C11, 3G7 (mouse)  70 5F7 (mouse)  71 12G6, 23E6 (mouse)  72 2C3 (mouse)  73 7F11 (mouse)  74 4B10 (mouse)  75 light chain primers Lead-ML kappa (forward primer in leader sequence)  76 FR1-ML kappa (forward primer in the framework 1)  77 ML kappa const (reverse primer in constant region)  78 VK-MK (forward primer in the framework 1)  79 MKC-Const (reverse primer in constant region)  80 heavy chain primers MH-SP-ALT1 (forward primer in leader sequence)  81 MH-SP-ALT2 (forward primer in leader sequence)  82 MH-FR1 (forward primer in the framework 1)  83 MH-FR1-1 (forward primer in the framework 1)  84 MH-J2 (reverse primer in J region)  85 MH-gamma-const (reverse primer in constant region)  86 VH MH1 (forward primer in the framework 1)  87 VH MH2 (forward primer in the framework 1)  88 VH MH3 (forward primer in the framework 1)  89 VH MH4 (forward primer in the framework 1)  90 VH MH5 (forward primer in the framework 1)  91 VH MH6 (forward primer in the framework 1)  92 VH MH7 (forward primer in the framework 1)  93 IgG1 (reverse primer in mouse IgG1 CH1 constant region)  94 IgG2A (reverse primer in mouse IgG2A CH1 constant region)  95 IgG2B (reverse primer in mouse IgG2B CH1 constant region)  96 VH (partial) 4B10 (mouse): alignment  97 human germline (VH) VH3-72: alignment  98 VH (partial) 4B10 (humanized): alignment  99 mouse VL (partial) 4B10 (mouse): alignment 100 human germline (VL) VK2-A18b: alignment 101 VL (partial) 4B10 (humanized): alignment 102 VL 4B10-VK1 (humanized) 103 VH 4B10-VH1 (humanized) 104 CD52 alanine-scanning WT 105 mutant peptides MUT 1 106 MUT 2 107 MUT 3 108 MUT 4 109 MUT 5 110 MUT 6 111 MUT 7 112 MUT 8 113 MUT 9 114 MUT 10 115 LC CDR-1 K/RSSQSLLN/IXS/TN/DGXS/TYLX 116 K/RSSQSLLN/IHS/TNGXS/TYLH 117 RSSQSLVHTNGNS/TYLH 118 LC CDR-2 XVSXXXS 119 XVSXRXS 120 MVSXRFS 121 LC CDR-3 XQXXH/R/KF/LN/IXX 122 SQSXH/R/KF/LN/IPX 123 SQSXHVPF/P 124 HC CDR-1 GFXFXXYW/YMX 125 GFTFXXYW/YMX 126 GFTFTDYW/YMS 127 HC CDR-2 XIRXKXBXYXTXYXXSVKG 128 XIRXKXNXYTTEYXXSVKG 129 FIRNKANGYTTEYXXSVKG 130 HC CDR-3 TXXXY/F/W 131 TRYXY/F/WFDY 132 TRYIF/WFDY 133 JH6 WGQGTTVTVSS 134 JK2 FGQGTKLEIK 135 JK5 FGQGTRLEIK 136 VH SFD1 7F11 137 SFD2 138 VL VK2 139 VH SFD1 2C3 140 12 141 15 142 16 143 17 144 19 145 VL VK1 146 VK11 147 VK12 148 VK13 149 VH SFD1 12G6 150 VH10 151 VH11 152 VH12 153 VL VK1 154 VK10 155 VK11 156 VK12 157 VK13 158 VH VH10 9D9 159 VH11 160 VH15 161 VH16 162 VH17 163 VH18 164 VL VK2 165 VK12 166 VK13 167 VK14 168 VK15 169 CD52 alanine-scanning MUT 1 170 peptides MUT 2 171 MUT 3 172 MUT 4 173 MUT 5 174 MUT 6 175 MUT 7 176 MUT 8 177 MUT 9 178 MUT 10 179 MUT 11 180 MUT 12 181 WT1 182 WT2 183 Tetanus toxoid HLA-DR- DTIMMEPPYCKGLDIYYKA 184 binding peptides SAMLTNLIIFGPGPVLNKNEV 185 NNFTVSFWLRVPKVSASHLE 186 ″irrelevant″ HLA-DR- CS 378-398 binding peptide 187 Campath-1H ®  978 188 LC overlapping 15-mer  979 189 peptides for  980 190 immunogenicity study  981 191  982 192  983 193  984 194  985 195  986 196  987 197  988 198  999 199  990 200  991 201  992 202  993 203  994 204  995 205  996 206  997 207 Campath-1H ®  998 208 HC overlapping 15-  999 209 mer peptides for 1000 210 immunogenicity study 1001 211 1002 212 1003 213 1004 214 1005 215 1006 216 1007 217 1008 218 1009 219 1010 220 1011 221 1012 222 1013 223 1014 224 1015 225 1016 226 1017 227 1018 228 1019 229 1020 230 12G6-SFD1/K12 1027 231 LC 1028 232 overlapping 15-mer 1029 233 peptides for 1030 234 immunogenicity study 1031 235 1032 236 1072 237 1073 238 1074 239 1036 240 1037 241 1038 242 1039 243 1040 244 1041 245 1042 246 1043 247 1075 248 1076 249 1077 250 1078 251 12G6-SFD1/K12 1048 252 HC 1049 253 overlapping 15-mer 1050 254 peptides for 1079 255 immunogenicity study 1080 256 1081 257 1082 258 1055 259 1056 260 1060 261 1061 262 1062 263 1063 264 1064 265 1065 266 1066 267 1067 268 1068 269 1083 270 1084 271 1085 272 HC 2C3-SFD1 2C3 273 LC 2C3-K12 274 HC 7F11-SFD1 7F11 275 LC 7F11-K2 276 HC 9D9-H16 9D9 277 9D9-H18 278 LC 9D9-K13 279 HC 12G6-SFD1 12G6 280 LC 12G6-K12 281 HC 4B10-H1 4B10 282 LC 4B10-K1 283 HC (nucleic acid) 2C3-SFD1 2C3 284 LC (nucleic acid) 2C3-K12 285 HC (nucleic acid) 7F11-SFD1 7F11 286 LC (nucleic acid) 7F11-K2 287 HC (nucleic acid) 9D9-H16 9D9 288 9D9-H18 289 LC (nucleic acid) 9D9-K13 290 HC (nucleic acid) 12G6-SFD1 12G6 291 LC (nucleic acid) 12G6-K12 292 HC (nucleic acid) 4B10-H1 4B10 293 LC (nucleic acid) 4B10-K1 294 HC CDR-3 7F11-SFD2 (ARYIFFDY) 7F11

The teachings of all patents, published applications and references cited herein are incorporated by reference in their entirety.

While this invention has been particularly shown and described with references to example embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the scope of the invention encompassed by the appended claims. 

1. A monoclonal anti-human CD52 antibody or an antigen-binding portion thereof, wherein the light chain and heavy chain of said antibody comprise the three complementarity determining regions (CDRs) found in a) SEQ ID NOs: 3 and 16, respectively; b) SEQ ID NOs: 4 and 17, respectively; c) SEQ ID NOs: 5 and 18, respectively; d) SEQ ID NOs: 6 and 19, respectively; e) SEQ ID NOs: 7 and 20, respectively; f) SEQ ID NOs: 8 and 21, respectively; g) SEQ ID NOs: 9 and 22, respectively; h) SEQ ID NOs: 10 and 23, respectively; i) SEQ ID NOs: 11 and 24, respectively; j) SEQ ID NOs: 12 and 25, respectively; k) SEQ ID NOs: 12 and 137, respectively; or l) SEQ ID NOs: 13 and 26, respectively.
 2. A monoclonal anti-human CD52 antibody, or an antigen-binding portion thereof, that binds to the same epitope on human CD52 as an anti-human CD52 antibody whose light chain and heavy chain comprise the three complementarity determining regions (CDRs) found in a) SEQ ID NOs: 3 and 16, respectively; b) SEQ ID NOs: 4 and 17, respectively; c) SEQ ID NOs: 5 and 18, respectively; d) SEQ ID NOs: 6 and 19, respectively; e) SEQ ID NOs: 7 and 20, respectively; f) SEQ ID NOs: 8 and 21, respectively; g) SEQ ID NOs: 9 and 22, respectively; h) SEQ ID NOs: 10 and 23, respectively; i) SEQ ID NOs: 11 and 24, respectively; j) SEQ ID NOs: 12 and 25, respectively; k) SEQ ID NOs: 12 and 137, respectively; or l) SEQ ID NOs: 13 and 26, respectively.
 3. A monoclonal anti-human CD52 antibody, or an antigen-binding portion thereof, that competes or cross-competes with an anti-human CD52 antibody whose light chain and heavy chain comprise the three complementarity determining regions (CDRs) found in a) SEQ ID NOs: 3 and 16, respectively; b) SEQ ID NOs: 4 and 17, respectively; c) SEQ ID NOs: 5 and 18, respectively; d) SEQ ID NOs: 6 and 19, respectively; e) SEQ ID NOs: 7 and 20, respectively; f) SEQ ID NOs: 8 and 21, respectively; g) SEQ ID NOs: 9 and 22, respectively; h) SEQ ID NOs: 10 and 23, respectively; i) SEQ ID NOs: 11 and 24, respectively; j) SEQ ID NOs: 12 and 25, respectively; k) SEQ ID NOs: 12 and 137, respectively; or l) SEQ ID NOs: 13 and 26, respectively. 4-24. (canceled)
 25. An isolated nucleic acid encoding the heavy chain or an antigen-binding portion thereof, or the light chain or an antigen-binding portion thereof, of the monoclonal antibody of claim
 1. 26-28. (canceled)
 29. A recombinant vector comprising (1) a nucleic acid sequence encoding the heavy chain or an antigen-binding portion thereof, (2) a nucleic acid sequence encoding the light chain or an antigen-binding portion thereof, or (3) both, of a monoclonal antibody according to claim
 1. 30. A host cell comprising a first nucleic acid sequence encoding the heavy chain or an antigen-binding portion thereof of a monoclonal antibody according to claim 1, said first nucleic acid sequence operably linked to an expression control element, and a second nucleic acid sequence encoding the light chain or an antigen-binding portion thereof of said monoclonal antibody, said second nucleic acid sequence operably linked to an expression control element.
 31. A method of making an anti-human CD52 antibody or an antigen-binding portion thereof, comprising maintaining the host cell of claim 30 under conditions appropriate for expression of the antibody or portion.
 32. (canceled)
 33. A composition comprising the monoclonal antibody or antigen-binding portion according to claim 1 and a pharmaceutically acceptable vehicle or carrier.
 34. A method for treating a patient in need thereof, comprising administering to the patient an effective amount of the monoclonal antibody or antigen-binding portion according to claim
 1. 35-54. (canceled) 